Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hearing and PLAT[original query] |
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Clinical characteristics of a Japanese family with hearing loss accompanied by compound heterozygous mutations in LOXHD1. Auris, nasus, larynx 2016 Mar . Minami Shujiro B, Mutai Hideki, Namba Kazunori, Sakamoto Hirozazu, Matsunaga Tats |
Recessive LOXHD1 variants cause a prelingual down-sloping hearing loss: genotype-phenotype correlation and three additional children with novel variants. International journal of pediatric otorhinolaryngology 2021 4 145 110715. Yu Sha, Chen Wen-Xia, Zhang Yun-Fei, Chen Chao, Ni Yihua, Duan Bo, Wang Huijun, Xu Zheng-M |
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- Page last updated:Apr 16, 2024
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