Concepedia

Publication | Open Access

Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

DOIFull Paper Access

153

Citations

28

References

2012

Year

Lijia Huang, Jodi Warman‐Chardon, Melissa T. Carter, K. Friend, Tracy Dudding, Jeremy Schwartzentruber, Ruobing Zou, Peter W. Schofield, Stuart Douglas, Dennis E. Bulman,
Orphanet Journal of Rare Diseases

References

YearCitations

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