ArticleNeurology2008
SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia.
C Paisan-Ruiz et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
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ArticleNeurology2008
C Paisan-Ruiz et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.