Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFA9 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to cytochrome c oxidase deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (COX15 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Isolated complex I deficiency) (NDUFS3 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to mitochondrial COX4 deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (COX10 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFA10 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome, 256000, Autosomal recessive, Mitochondrial; LS (Leigh syndrome) (BCS1L gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (SDHA gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to cytochrome c oxidase deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (COX15 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFS8 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFS7 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to mitochondrial complex 1 deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFA12 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFA2 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (FOXRED1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFAF2 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFS7 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (FOXRED1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to mitochondrial complex 1 deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFA12 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFAF2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFA10 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Leigh syndrome due to mitochondrial COX4 deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (COX10 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
