Novel loss of function mutations in Asian kindreds with hereditary spastic paraplegia and thin corpus callosurn (SPG11)

Detalles Bibliográficos
Autores principales:	Baumber, L, Patel, S, Kinning, E, Critchley, P, Nemeth, A, Talbot, K, Maher, E, Trembath, R
Formato:	Conference item
Publicado:	2007

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