PMC Articles for MedGen (Select 375052) - PMC

Result Filters

Links from MedGen

Items: 3

Select item 11803181.

Multiple Mutations of MYO1A, a Cochlear-Expressed Gene, in Sensorineural Hearing Loss

Francesca Donaudy, Antonella Ferrara, Laura Esposito, Ronna Hertzano, Orit Ben-David, Rachel E. Bell, Salvatore Melchionda, Leopoldo Zelante, Karen B. Avraham, Paolo Gasparini

Am J Hum Genet. 2003 Jun; 72(6): 1571–1577. Published online 2003 May 6. doi: 10.1086/375654

PMCID:: PMC1180318

Article PubReader PDF–363K Cite

Select item 65606362.

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

Li Wang, Yong Feng, Denise Yan, Litao Qin, M’hamed Grati, Rahul Mittal, Tao Li, Abhiraami Kannan Sundhari, Yalan Liu, Prem Chapagain, Susan H. Blanton, Shixiu Liao, Xuezhong Liu

Hum Genet. Author manuscript; available in PMC 2019 Jul 1.

Published in final edited form as: Hum Genet. 2018 Jul; 137(6-7): 437–446. Published online 2018 Jun 2. doi: 10.1007/s00439-018-1895-y