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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 10, 2024. (Total: 234259Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Amyotrophic Lateral Sclerosis and SIGMAR1[original query]
Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system.
Neurobiology of aging 2014 Dec 35 (12): 2881.e11-5.
Liu Zhi-Jun, Li Hong-Fu, Tan Guo-He, Tao Qing-Qing, Ni Wang, Cheng Xue-Wen, Xiong Zhi-Qi, Wu Zhi-Yi
Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis.
Neurobiology of aging 2014 Aug 35 (8): 1957.e7-8.
Kim Hee-Jung, Kwon Min-Jung, Choi Won-Jun, Oh Ki-Wook, Oh Seong-Il, Ki Chang-Seok, Kim Seung Hy
Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort.
Frontiers in genetics 2019 10 732.
Tripolszki Kornélia, Gampawar Piyush, Schmidt Helena, Nagy Zsófia F, Nagy Dóra, Klivényi Péter, Engelhardt József I, Széll Már
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