Detalhe da pesquisa
1.
No correlation between amount of aberrant transcript and severity of phenotype in hereditary spastic paraplegia patients with a c.1242A > G splice mutation in the SPG4 gene.
J Neurol
; 253(6): 804-5, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16362530