Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: AIFM1[original query] |
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Detergent Insoluble Proteins and Inclusion Body-Like Structures Immunoreactive for PRKDC/DNA-PK/DNA-PKcs, FTL, NNT, and AIFM1 in the Amygdala of Cognitively Impaired Elderly Persons. Journal of neuropathology and experimental neurology 2018 Jan 77 (1): 21-39. Gal Jozsef, Chen Jing, Katsumata Yuriko, Fardo David W, Wang Wang-Xia, Artiushin Sergey, Price Douglas, Anderson Sonya, Patel Ela, Zhu Haining, Nelson Peter |
Whole exome sequencing identifies a novel variant in an apoptosis-inducing factor gene associated with X-linked recessive hearing loss in a Chinese family. Genetics and molecular biology 2019 6 42 (3): 543-548. Wang Qi, Xingxing Lu, Ding Zhiwei, Qi Yu, Liu Yu |
High Frequency of AIFM1 Variants and Phenotype Progression of Auditory Neuropathy in a Chinese Population. Neural plasticity 2020 7 2020 5625768. Wang Hongyang, Bing Dan, Li Jin, Xie Linyi, Xiong Fen, Lan Lan, Wang Dayong, Guan Jing, Wang Qiu |
Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot. Translational pediatrics 2023 11 12 (10): 1835-1841. Yu Pan, Manli Liu, Songsong Zhang, Huaxian Mei, Jing |
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- Page last updated:Apr 22, 2024
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