X. Qin

Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse.

J. Haines, T. Lerner, T. Gillis, 2002, American journal of human genetics.

A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter

A. Pandya, X. Liu, S. Blanton, 2002, Journal of medical genetics.