Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: OXGR1[original query] |
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Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke. Stroke 2020 3 51 (4): 1056-1063. Ilinca Andreea, Martinez-Majander Nicolas, Samuelsson Sofie, Piccinelli Paul, Truvé Katarina, Cole John, Kittner Steven, Soller Maria, Kristoffersson Ulf, Tatlisumak Turgut, Puschmann Andreas, Putaala Jukka, Lindgren Ar |
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis. Genetics in medicine : official journal of the American College of Medical Genetics 2022 12 25 (3): 100351. Majmundar Amar J, Widmeier Eugen, Heneghan John F, Daga Ankana, Wu Chen-Han Wilfred, Buerger Florian, Hugo Hannah, Ullah Ihsan, Amar Ali, Ottlewski Isabel, Braun Daniela A, Jobst-Schwan Tilman, Lawson Jennifer A, Zahoor Muhammad Yasir, Rodig Nancy M, Tasic Velibor, Nelson Caleb P, Khaliq Shagufta, Schönauer Ria, Halbritter Jan, Sayer John A, Fathy Hanan M, Baum Michelle A, Shril Shirlee, Mane Shrikant, Alper Seth L, Hildebrandt Friedhe |
A whole exome sequencing study to identify rare variants in multiplex families with alcohol use disorder. Frontiers in psychiatry 2023 11 14 1216493. Shirley Y Hill, Joseph Host |
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- Page last updated:Apr 29, 2024
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