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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 GPM6B[original query]
PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: Identification of one partial triplication and two partial deletions of PLP1.
Neurogenetics 2006 Mar 7 (1): 31-7.
Combes Patricia, Bonnet-Dupeyron Marie-Noelle, Gauthier-Barichard Fernande, Schiffmann Raphael, Bertini Enrico, Rodriguez Diana, Armour John A L, Boespflug-Tanguy Odile, Vaurs-Barrière Catheri
Common X-Chromosome Variants Are Associated with Parkinson Disease Risk. GWAS Catalog
Annals of neurology 2021 Feb .
Le Guen Yann, Napolioni Valerio, Belloy Michael E, Yu Eric, Krohn Lynne, Ruskey Jennifer A, Gan-Or Ziv, Kennedy Gabriel, Eger Sarah J, Greicius Michael
Predominant monomorphism of the RIT2 and GPM6B exceptionally long GA blocks in human and enriched divergent alleles in the disease compartment.
Genetica 2022 1 150 (1): 27-40.
Khamse S, Arabfard M, Salesi M, Behmard E, Jafarian Z, Afshar H, Khazaei M, Ohadi
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