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)

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Hlavní autoři: Baumber, L, Patel, S, Kinning, E, Critchley, P, Nemeth, A, Talbot, K, Maher, E, Trembath, R
Médium: Conference item
Vydáno: 2007

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