A Family with Vocal Cord Paralysis Associated with GDAP1 Mutation in Giresun, Turkey
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چکیده
منابع مشابه
a novel mutation of gdap1 associated with charcot-marie-tooth disease in an iranian family
as a result of higher distributed consanguinity in the mediterranean region and the middle east, autosomal-recessive forms of charcot-marie-tooth (arcmt) are more common in these areas. cmt disease caused by mutations in the ganglioside-induced differentiation-associated protein 1 (gdap1) gene is a severe autosomal recessive neuropathy resulting in either demyelinating cmt4a neuropathy or axona...
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ژورنال
عنوان ژورنال: Türk Nöroloi Dergisi
سال: 2015
ISSN: 1301-062X
DOI: 10.4274/tnd.38358