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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and SLC12A6[original query]
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
Brain : a journal of neurology 2015 Nov .
Montecchiani Celeste, Pedace Lucia, Lo Giudice Temistocle, Casella Antonella, Mearini Marzia, Gaudiello Fabrizio, Pedroso José L, Terracciano Chiara, Caltagirone Carlo, Massa Roberto, St George-Hyslop Peter H, Barsottini Orlando G P, Kawarai Toshitaka, Orlacchio Anton
Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. GWAS Catalog
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2018 Mar .
Dong Jing, Levine David M, Buas Matthew F, Zhang Rui, Onstad Lynn, Fitzgerald Rebecca C, , Corley Douglas A, Shaheen Nicholas J, Lagergren Jesper, Hardie Laura J, Reid Brian J, Iyer Prasad G, Risch Harvey A, Caldas Carlos, Caldas Isabel, Pharoah Paul D, Liu Geoffrey, Gammon Marilie D, Chow Wong-Ho, Bernstein Leslie, Bird Nigel C, Ye Weimin, Wu Anna H, Anderson Lesley A, MacGregor Stuart, Whiteman David C, Vaughan Thomas L, Thrift Aaron
SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population.
Human genetics 2021 11 141 (1): 81-99.
Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous
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