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probable G-protein coupled receptor 139 isoform 1 [Homo sapiens]
probable G-protein coupled receptor 139 isoform 1 [Homo sapiens]
gi|50897278|ref|NP_001002911.1|
Protein
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Peroxisomal Disorders
Peroxisomal Disorders
A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthet...<br/>Year introduced: 1996
MeSH
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Myotonic Disorders
Myotonic Disorders
Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized ...<br/>Year introduced: 2000
MeSH
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