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Publications by W.H. Feng
Mutation Analysis of Four Chinese Families With Pure Hereditary Spastic Paraplegia: Pseudo- X-Linked Dominant Inheritance and Male Lethality Due to a Novel ATL1 Mutation
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
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Novel Homozygous GBA2 Mutation in a Patient With Complicated Spastic Paraplegia
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A Hereditary Spastic Paraplegia Mutation in Kinesin-1a/Kif5a Disrupts Neurofilament Transport
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Autosomal Dominant Hereditary Spastic Paraplegia: Novel Mutations in the REEP1 Gene (SPG31)
BMC Medical Genetics
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X-Linked Spastic Paraplegia Type 34
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Schweizer Archiv für Neurologie und Psychiatrie
Three Novel Mutations of the Spastin Gene in Chinese Patients With Hereditary Spastic Paraplegia
Archives of Neurology
Hereditary Spastic Paraplegia SPG13 Is Associated With a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60
American Journal of Human Genetics
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The Hsp60-(p.V98I) Mutation Associated With Hereditary Spastic Paraplegia SPG13 Compromises Chaperonin Function Bothin Vitroandin Vivo
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Extensive in Silico Analysis of ATL1 Gene : Discovered Five Mutations That May Cause Hereditary Spastic Paraplegia Type 3A
Scientifica
Agricultural
Environmental Science
Biological Sciences
