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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)
2007
L Baumber
S Patel
Esther Kinning
Peter Critchley
Andrea H. Németh
Kevin Talbot
Eamonn R. Maher
Richard C. Trembath
Keywords:
Genetics
Hereditary spastic paraplegia
Biology
Cancer research
Loss function
Correction
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