Analysis of autosomal dominant spinocerebellar ataxia type 1 in an extended family of central India

Conclusion: We found the clinical (symptoms and MRI) and genetic (Pedigree and PCR) results to be correlated. The PCR result revealed the disease to be of SCA 1 type being inherited in the family.
Source: Indian Journal of Human Genetics - Category: Genetics & Stem Cells Authors: Source Type: research