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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 SLC26A8[original query]
A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12.
PloS one 2015 10 (8): e0134720.
Bianchi Matteo, Dahlgren Stina, Massey Jonathan, Dietschi Elisabeth, Kierczak Marcin, Lund-Ziener Martine, Sundberg Katarina, Thoresen Stein Istre, Kämpe Olle, Andersson Göran, Ollier William E R, Hedhammar Åke, Leeb Tosso, Lindblad-Toh Kerstin, Kennedy Lorna J, Lingaas Frode, Rosengren Pielberg Ger
Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.
Human mutation 2021 12 43 (3): 434-443.
Gao Yang, Wu Huan, Xu Yuping, Shen Qunshan, Xu Chuan, Geng Hao, Lv Mingrong, Tan Qing, Li Kuokuo, Tang Dongdong, Song Bing, Zhou Ping, Wei Zhaolian, He Xiaojin, Cao Yunx
Genetic susceptibility to temporomandibular joint involvement in juvenile idiopathic arthritis.
Journal of oral rehabilitation 2024 8 .
P Niibo, T Nikopensius, T Jagomägi, Ü Voog, T Haller, N Tõnisson, A Metspalu, M Saag, C Pruunsi
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