Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Deafness and PDZD7[original query] |
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Novel recessive PDZD7 biallelic mutations in two Chinese families with non-syndromic hearing loss. American journal of medical genetics. Part A 2017 10 176 (1): 99-106. Guan Jing, Wang Hongyang, Lan Lan, Wang Li, Yang Ju, Xie Linyi, Yin Zifang, Xiong Wenping, Zhao Lidong, Wang Dayong, Wang Qiu |
Targeted next-generation sequencing of deaf patients from Southwestern China. Molecular genetics & genomic medicine 2021 Mar e1660. Li Yunlong, Su Jie, Zhang Jingman, Pei Jiahong, Li Dongmei, Zhang Yinhong, Li Jingyu, Chen Menglang, Zhu Baoshe |
Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes. Orphanet journal of rare diseases 2022 3 17 (1): 114. Mutai Hideki, Momozawa Yukihide, Kamatani Yoichiro, Nakano Atsuko, Sakamoto Hirokazu, Takiguchi Tetsuya, Nara Kiyomitsu, Kubo Michiaki, Matsunaga Tats |
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