Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Syndrome and ABHD12[original query] |
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Novel ABHD12 mutations in PHARC patients: the differential diagnosis of deaf-blindness. The Annals of otology, rhinology, and laryngology 2015 May 124 Suppl 1 77S-83S. Yoshimura Hidekane, Hashimoto Takao, Murata Toshinori, Fukushima Kunihiro, Sugaya Akiko, Nishio Shin-Ya, Usami Shin-Ic |
Comprehensive Molecular Screening in Chinese Usher Syndrome Patients. Investigative ophthalmology & visual science 2018 Mar 59 (3): 1229-1237. Sun Tengyang, Xu Ke, Ren Yanfan, Xie Yue, Zhang Xiaohui, Tian Lu, Li Ya |
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- Page last updated:Apr 22, 2024
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