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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 23, 2025. (Total: 235602Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Atrophy and CISD2[original query]
Genotypic classification of patients with Wolfram syndrome: insights into the natural history of the disease and correlation with phenotype.
Genetics in medicine : official journal of the American College of Medical Genetics 2013 Jul 15 (7): 497-506.
de Heredia Miguel López, Clèries Ramón, Nunes Virgin
Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome.
BMC endocrine disorders 2021 8 21 (1): 166.
Ren Ziyu, Yi Jixiu, Zhong Min, Wang Yunting, Liu Qicong, Wang Xuan, Liu Dongfang, Ren W
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