Shirong Zhang

T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.

Mugen Liu, Q. Wang, Lejin Wang, 2008, Mitochondrion.

Mutation c.359_363delGTATTinsATAC in the COL4A5 causes Alport syndrome in a Chinese family.

Qing Wang, Mugen Liu, Zhao-hui Tang, 2013, Gene.

Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family

Mugen Liu, Q. Wang, X. Ren, 2008, BMC Medical Genetics.

Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family

Mugen Liu, Q. Wang, Lejin Wang, 2008, Molecular vision.

Ser217Cys mutation in the Ig II domain of FGFR3 in a Chinese family with autosomal dominant achondroplasia.

Qing Wang, Mugen Liu, X. Ren, 2007, Chinese medical journal.

Bmc Medical Genetics Identification of a Novel Kcnq1 Mutation Associated with Both Jervell and Lange-nielsen and Romano-ward Forms of Long Qt Syndrome in a Chinese Family

Mugen Liu, Q. Wang, X. Ren, 2022 .