CW Fung

<i><scp>NDUFA9</scp></i> point mutations cause a variable mitochondrial complex I assembly defect

Fabian Baertling, Laura Sánchez‐Caballero, M.A.M. van den Brand et al. · Clinical Genetics · 2017 · 45 citations · Full text

COG5-CDG with a Mild Neurohepatic Presentation

CW Fung, Gert Matthijs, Luisa Sturiale et al. · JIMD Reports · 2011 · 35 citations · Full text

<scp>MALDI‐MS</scp> profiling of serum <i>O</i>‐glycosylation and <i>N</i>‐glycosylation in <scp>COG5‐CDG</scp>

Angelo Palmigiano, Rosaria Ornella Bua, Rita Barone et al. · Journal of Mass Spectrometry · 2017 · 23 citations

Megaconial congenital muscular dystrophy: Same novel homozygous mutation in CHKB gene in two unrelated Chinese patients

H.S. Chan, Ronnie SL Ho, PL Khong et al. · Neuromuscular Disorders · 2019 · 14 citations

Unrelated Chinese Patients, Rare Diseases, Developmental Biology +10