Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis.
Chorea-acanthocytosis (ChAc) is an autosomal recessive neurological disorder whose characteristic features include hyperkinetic movements and abnormal red blood cell morphology. Mutations in the CHAC gene on 9q21 were recently found to cause chorea-acanthocytosis. CHAC encodes a large, novel protein...
المؤلفون الرئيسيون: | Dobson-Stone, C, Danek, A, Rampoldi, L, Hardie, R, Chalmers, R, Wood, N, Bohlega, S, Dotti, M, Federico, A, Shizuka, M, Tanaka, M, Watanabe, M, Ikeda, Y, Brin, M, Goldfarb, L, Karp, B, Mohiddin, S, Fananapazir, L, Storch, A, Fryer, A, Maddison, P, Sibon, I, Trevisol-Bittencourt, P, Singer, C, Caballero, I |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2002
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مواد مشابهة
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Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis
حسب: Dobson-Stone, C, وآخرون
منشور في: (2002) -
Chorein detection for the diagnosis of chorea-acanthocytosis.
حسب: Dobson-Stone, C, وآخرون
منشور في: (2004) -
Mutation in the CHAC gene in a family of autosomal dominant chorea-acanthocytosis.
حسب: Walker, R, وآخرون
منشور في: (2012) -
Identification and characterisation of the gene for chorea-acanthocytosis.
حسب: Rampoldi, L, وآخرون
منشور في: (2001) -
Genomic organization of the human galpha14 and Galphaq genes and mutation analysis in chorea-acanthocytosis (CHAC).
حسب: Rubio, J, وآخرون
منشور في: (1999)