ArticleNeurogenetics2007
SPG11: a consistent clinical phenotype in a family with homozygous spatacsin truncating mutation.
Roberto Del Bo et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
16 papers cite it
this papercites it
ArticleNeurogenetics2007
Roberto Del Bo et al.PubMed ↗Publisher ↗
No numbers read from the abstract.