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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 - 2 (of 2 Records)

Query Trace: Disease and CLCA2[original query]
Identification of risk loci for Crohn's disease phenotypes using a genome-wide association study. GWAS Catalog
Gastroenterology 2015 Apr 148 (4): 794-805.
Alonso Arnald, Domènech Eugeni, Julià Antonio, Panés Julián, García-Sánchez Valle, Mateu Pilar Nos, Gutiérrez Ana, Gomollón Fernando, Mendoza Juan L, Garcia-Planella Esther, Barreiro-de Acosta Manuel, Muñoz Fernando, Vera Maribel, Saro Cristina, Esteve Maria, Andreu Montserrat, Chaparro Maria, Manyé Josep, Cabré Eduard, López-Lasanta María, Tortosa Raül, Gelpí Josep Lluís, García-Montero Andrés C, Bertranpetit Jaume, Absher Devin, Myers Richard M, Marsal Sara, Gisbert Javier
A newly identified missense mutation in CLCA2 is associated with autosomal dominant cardiac conduction block.
Gene 2019 7 714 143990.
Mao Zhuo, Wang Yi, Peng Hao, He Fang, Zhu Li, Huang He, Huang Xianghong, Lu Xiaowei, Tan Xiaoj
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