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STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
Heimdal, Ketil, Sanchez-Guixé, Monica, Aukrust, Ingvild, Bollerslev, Jens, Bruland, Ove, Jablonski, Greg, Erichsen, Anne, Gude, Einar, Koht, Jeanette A, Erdal, Sigrid, Fiskerstrand, Torunn, Haukanes,Volume:
9
Year:
2014
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-014-0146-0
File:
PDF, 1.01 MB
english, 2014