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

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

Библиографические подробности
Главные авторы:	Baumber, L, Patel, S, Kinning, E, Critchley, P, Nemeth, A, Talbot, K, Maher, E, Trembath, R
Формат:	Conference item
Опубликовано:	2007

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