Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia
A. K. Erichsen, E. Inderhaug, M. Mattingsdal, K. Eiklid, C. M. E. TallaksenVolume:
14
Year:
2007
Language:
english
Pages:
6
DOI:
10.1111/j.1468-1331.2007.01861.x
File:
PDF, 504 KB
english, 2007