Papers: 10.1186/1750-1172-7-67

https://doi.org/10.1186/1750-1172-7-67

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

Cited by: 116
Author(s): Lijia Huang, Jodi Warman‐Chardon, Melissa T. Carter, K. Friend, Tracy Dudding, Jeremy Schwartzentruber, Ruobing Zou, Peter R. Schofield, Stuart Douglas, Dennis E. Bulman, Kym M. Boycott
Published: about 14 years ago

Software Mentions 1