Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: EIF2B3[original query] |
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Investigation of the PARK10 gene in Parkinson disease. Annals of human genetics 2007 Sep 71 (Pt 5): 639-47. Li Y J, Deng J, Mayhew G M, Grimsley J W, Huo X, Vance J |
Association mapping of the PARK10 region for Parkinson's disease susceptibility genes. Parkinsonism & related disorders 2014 Jan 20 (1): 93-8. Wan Jia Y, Edwards Karen L, Hutter Carolyn M, Mata Ignacio F, Samii Ali, Roberts John W, Agarwal Pinky, Checkoway Harvey, Farin Federico M, Yearout Dora, Zabetian Cyrus |
Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention. Journal of ovarian research 2020 9 13 (1): 114. Liu Hongli, Wei Xiaoli, Sha Yanwei, Liu Wensheng, Gao Haijie, Lin Jin, Li Youzhu, Tang Yaling, Wang Yifeng, Wang Yanlong, Su Zhiyi |
Case Report: A Novel EIF2B3 Pathogenic Variant in Central Nervous System Hypomyelination/Vanishing White Matter. Frontiers in genetics 2022 7 13 893057. Wongkittichote Parith, Mar Soe Soe, McKinstry Robert C, Nguyen Hoa |
Diagnostic yield of clinical exome sequencing in adulthood in medical genetics clinics. American journal of medical genetics. Part A 2022 11 191 (2): 510-517. Mainali Apurba, Athey Taryn, Bahl Shalini, Hung Clara, Caluseriu Oana, Chan Alicia, Eaton Alison, Ghai Shailly Jain, Kannu Peter, MacPherson Melissa, Niederhoffer Karen Y, Siriwardena Komudi, Mercimek-Andrews Saad |
Genotypic and phenotypic heterogeneity among Chinese pediatric genetic white matter disorders. Italian journal of pediatrics 2023 11 49 (1): 155. Liling Dong, Li Shang, Caiyan Liu, Chenhui Mao, Xinying Huang, Shanshan Chu, Bin Peng, Liying Cui, Jing G |
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