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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 3, 2024. (Total: 232098Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Sclerosis and C7[original query]
Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.
Human molecular genetics 2009 May 18 (9): 1670-83.
Kallio Suvi P, Jakkula Eveliina, Purcell Shaun, Suvela Minna, Koivisto Keijo, Tienari Pentti J, Elovaara Irina, Pirttilä Tuula, Reunanen Mauri, Bronnikov Denis, Viander Markku, Meri Seppo, Hillert Jan, Lundmark Frida, Harbo Hanne F, Lorentzen Aslaug R, De Jager Philip L, Daly Mark J, Hafler David A, Palotie Aarno, Peltonen Leena, Saarela Jan
The complement C7 variant rs3792646 is associated with amyotrophic lateral sclerosis in a Han Chinese population.
Neurobiology of aging 2020 Nov .
He Ji, Fu Jiayu, Fan Dongshe
Rare DNAJC7 Variants May Play a Minor Role in Chinese Patients with ALS.
Molecular neurobiology 2023 10 .
Shichan Wang, Xiaoting Zheng, Qianqian Wei, Junyu Lin, Tianmi Yang, Yi Xiao, Qirui Jiang, Chunyu Li, Huifang Sha
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