SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia
C. Paisan-Ruiz
, O. Dogu
, A. Yilmaz
, H. Houlden
, A. Singleton
Research output: Contribution to journal › Article › peer-review
71Scopus
citations
Fingerprint
Dive into the research topics of 'SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia'. Together they form a unique fingerprint.