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Year | Number of Results |
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2001 | 2 |
2019 | 1 |
2024 | 0 |
PubMed (cited) for id: 611978
3 results
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A variant in MRPS14 (uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement.
Hum Mol Genet. 2019 Feb 15;28(4):639-649. doi: 10.1093/hmg/ddy374.
Hum Mol Genet. 2019.
PMID: 30358850
Free article.
The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders.
Kenmochi N, Suzuki T, Uechi T, Magoori M, Kuniba M, Higa S, Watanabe K, Tanaka T.
Kenmochi N, et al.
Genomics. 2001 Sep;77(1-2):65-70. doi: 10.1006/geno.2001.6622.
Genomics. 2001.
PMID: 11543634
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The small subunit of the mammalian mitochondrial ribosome. Identification of the full complement of ribosomal proteins present.
Cavdar Koc E, Burkhart W, Blackburn K, Moseley A, Spremulli LL.
Cavdar Koc E, et al.
J Biol Chem. 2001 Jun 1;276(22):19363-74. doi: 10.1074/jbc.M100727200. Epub 2001 Mar 2.
J Biol Chem. 2001.
PMID: 11279123
Free article.
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