W. Hwu

Six novel NPC1 mutations in Chinese patients with Niemann–Pick disease type C

W. Hwu, Chih-Chao Yang, Ming‐Jen Lee, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

Identification and characterization of ‐3c–g acceptor splice site mutation in human α‐ l‐iduronidase associated with mucopolysaccharidosis type IH/S

T.-R. Wang, G. Lee-Chen, Sp Lin, 2000, Clinical Genetics.

Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency

C. Manegold, W. Hwu, M. Verbeek, 2010, Neurology.

Valproic acid treatment in six patients with spinal muscular atrophy

L. Tsai, C. Yang, W. Hwu, 2007, European journal of neurology.

DNA Haplotype Analysis of CAG Repeat in Taiwanese Huntington’s Disease Patients

K. Gwinn‐Hardy, W. Hwu, Yih-Ru Wu, 2004, European Neurology.

Two novel mutations in the α‐galactosidase A gene in Chinese patients with Fabry disease

W. Hwu, L. Lai, Y. Lien, 2003 .