Ilene Chiu

发表

Mutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89.

Lana M. Pollock, M. Adams, D. Nickerson, 2013, American journal of human genetics.

Role of the CCAAT-Binding Protein NFY in SCA17 Pathogenesis

Chung-Hsin Wu, Guan-Chiun Lee, H. Hsieh-Li, 2012, PloS one.

A Point Mutation in the Gene for Asparagine-Linked Glycosylation 10B (Alg10b) Causes Nonsyndromic Hearing Impairment in Mice (Mus musculus)

Simon S. Gao, M. Justice, D. del Gaudio, 2013, PloS one.

Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish.

J. Shendure, D. Nickerson, S. Leal, 2014, Human molecular genetics.