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)

מידע ביבליוגרפי
Main Authors: Baumber, L, Patel, S, Kinning, E, Critchley, P, Nemeth, A, Talbot, K, Maher, E, Trembath, R
פורמט: Conference item
יצא לאור: 2007

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