Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: CLCA2[original query] |
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Identification of risk loci for Crohn's disease phenotypes using a genome-wide association study.
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 |
Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians.
Journal of foot and ankle research 2020 Mar 13 (1): 11. Arbeeva Liubov, Yau Michelle, Mitchell Braxton D, Jackson Rebecca D, Ryan Kathleen, Golightly Yvonne M, Hannan Marian T, Nelson Amanda, Jordan Joanne M, Hochberg Marc |
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