Spinocerebellar ataxia type 7 (SCA7) – correlations between phenotype and genotype in one large Belgian family
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference30 articles.
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3. Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion;Del-Favero;Hum Mol Genet,1998
4. Autosomal dominant cone dystrophy–cerebellar atrophy (ADCoCA) (modified ADCA Harding II);Neetens;Neuro-Ophthalmology,1990
5. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1;Benomar;Nat Genet,1995
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