One mutation, two phenotypes: a single nonsense mutation of theCTSCgene causes two clinically distinct phenotypes
نویسندگان
چکیده
منابع مشابه
A Novel Nonsense mutation in PANK2 Gene in Two Patients with Pantothenate Kinase-Associated Neurodegeneration
Pantothenate kinase- associated neurodegeneration (PKAN) syndrome is a rare autosomal recessive disorder characterized by progressive extrapyramidal dysfunction and iron accumulation in the brain and axonal spheroids in the central nervous system. It has been shown that the disorder is caused by mutations in PANK2 gene which codes for a mitochondrial enzyme participating in coenzyme A biosynthe...
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ژورنال
عنوان ژورنال: Clinical and Experimental Dermatology
سال: 2015
ISSN: 0307-6938
DOI: 10.1111/ced.12710