H. Kwon

A cystic fibrosis patient with two novel mutations in mitochondrial DNA: mild disease led to delayed diagnosis of both disorders.

A. Gropman, L. Wong, M. Liang, 2002, American journal of medical genetics.

A novel mutation in the mitochondrial tRNASer(AGY) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency

D. Kerr, C. Hoppel, L. Wong, 2006, Journal of Medical Genetics.

Mitochondrial DNA mutations in a patient with sex reversal and clinical features consistent with Fraser syndrome

L. Wong, H. Kwon, P. Suwannarat, 2005, Clinical genetics.

Hearing Loss in Mitochondrial Disorders

Lee-Jun C Wong, Cherng-Lih Perng, L. Wong, 2005, Annals of the New York Academy of Sciences.

Comprehensive scanning of the entire mitochondrial genome for mutations.

L. Wong, M. Liang, D. Tan, 2002, Clinical chemistry.

Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy

A. Gropman, F. Scaglia, A. Feigenbaum, 2006, Genetics in Medicine.

Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness

B. Robinson, A. Feigenbaum, L. Wong, 2006, American journal of medical genetics. Part A.