Progressive Dominant Hearing Loss (Autosomal Dominant Deafness‐41) and P2RX2 Gene Mutations: A Phenotype–Genotype Study

Collaboration types: Domestic collaboration; International collaboration
Citation topics: 1 Clinical & Life Sciences; 1.150 Hearing Loss; 1.150.421 Cochlea
Web Of Science research areas: Medicine, Research & Experimental; Otorhinolaryngology
ESI research areas: Clinical Medicine

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Source: InCites

Title: Progressive Dominant Hearing Loss (Autosomal Dominant Deafness‐41) and P2RX2 Gene Mutations: A Phenotype–Genotype Study
Creators: Xue Zhong Liu - Department of OtolaryngologyUniversity of Miami Miller School of Medicine Miami Florida U.S.A., Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human GeneticsUniversity of Miami Miller School of Medicine Miami Florida U.S.A
Denise Yan - Department of OtolaryngologyUniversity of Miami Miller School of Medicine Miami Florida U.S.A
Rahul Mittal - Department of OtolaryngologyUniversity of Miami Miller School of Medicine Miami Florida U.S.A
Megan E Ballard - Department of OtolaryngologyUniversity of Miami Miller School of Medicine Miami Florida U.S.A
Yong Feng - Department of Otolaryngology, Xiangya HospitalCentral South University Changsha China
Publication Details: The Laryngoscope, Vol.130(7), pp.1657-1663
Academic Unit: Miller School of Medicine; UMMG Department of Otolaryngology
Language: English
Resource Type: Journal article
PMID: 31593348
Record Identifier: 991031578520702976