共 50 条
- [41] Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix-Saguenay, ARSACS, in a Finnish family CLINICAL CASE REPORTS, 2016, 4 (12): : 1151 - 1156
- [42] STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity ORPHANET JOURNAL OF RARE DISEASES, 2014, 9 : 146
- [44] Novel compound heterozygous DPH1 mutations in a patient with the unique clinical features of airway obstruction and external genital abnormalities Journal of Human Genetics, 2018, 63 : 529 - 532
- [49] Novel Compound Heterozygous CBS Mutations Cause Homocystinuria in a Han Chinese Family Scientific Reports, 5
- [50] Clinical features and genetic analysis of a Spanish family with spinocerebellar ataxia 6 ACTA NEUROLOGICA SCANDINAVICA, 1999, 99 (01): : 43 - 47