Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: NAA10[original query] |
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Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups. Annals of the rheumatic diseases 2013 Mar 72 (3): 437-44. Kaufman Kenneth M, Zhao Jian, Kelly Jennifer A, Hughes Travis, Adler Adam, Sanchez Elena, Ojwang Joshua O, Langefeld Carl D, Ziegler Julie T, Williams Adrienne H, Comeau Mary E, Marion Miranda C, Glenn Stuart B, Cantor Rita M, Grossman Jennifer M, Hahn Bevra H, Song Yeong Wook, Yu Chack-Yung, James Judith A, Guthridge Joel M, Brown Elizabeth E, Alarcón Graciela S, Kimberly Robert P, Edberg Jeffrey C, Ramsey-Goldman Rosalind, Petri Michelle A, Reveille John D, Vilá Luis M, Anaya Juan-Manuel, Boackle Susan A, Stevens Anne M, Freedman Barry I, Criswell Lindsey A, Pons Estel Bernardo A, , Lee Joo-Hyun, Lee Ji-Seon, Chang Deh-Ming, Scofield R Hal A, Gilkeson Gary S, Merrill Joan T, Niewold Timothy B, Vyse Timothy James, Bae Sang-Cheol, Alarcón-Riquelme Marta E, , Jacob Chaim O, Moser Sivils Kathy, Gaffney Patrick M, Harley John B, Sawalha Amr H, Tsao Betty |
A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy. European journal of human genetics : EJHG 2018 5 26 (9): 1294-1305. Støve Svein Isungset, Blenski Marina, Stray-Pedersen Asbjørg, Wierenga Klaas J, Jhangiani Shalini N, Akdemir Zeynep Coban, Crawford David, McTiernan Nina, Myklebust Line M, Purcarin Gabriela, McNall-Knapp Rene, Wadley Alexandrea, Belmont John W, Kim Jeffrey J, Lupski James R, Arnesen Thom |
Targeted next generation sequencing in 112 Chinese patients with intellectual disability/developmental delay: novel mutations and candidate gene. BMC medical genetics 2019 5 20 (1): 80. Yan Huifang, Shi Zhen, Wu Ye, Xiao Jiangxi, Gu Qiang, Yang Yanling, Li Ming, Gao Kai, Chen Yinyin, Yang Xiaoping, Ji Haoran, Cao Binbin, Duan Ruoyu, Jiang Yuwu, Wang Jingm |
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- Page last updated:Mar 25, 2024
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