Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: AMPD3[original query] |
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A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3. Human mutation 2001 1 17 (1): 78. Yamada Y, Goto H, Wakamatsu N, Ogasawara |
Meta-analysis of genome-wide association studies identifies three novel loci for saturated fatty acids in East Asians. European journal of nutrition 2017 Jun 56 (4): 1477-1484. Zhu Jingwen, Manichaikul Ani, Hu Yao, Chen Yii-Der I, Liang Shuang, Steffen Lyn M, Rich Stephen S, Tsai Michael, Siscovick David S, Lemaitre Rozenn N, Li Huaixing, Lin |
Genetic contribution to lipid levels in early life based on 158 loci validated in adults: the FAMILY study. Scientific reports 2017 Dec 7 (1): 68. Christie Shanice, Robiou-du-Pont Sébastien, Anand Sonia S, Morrison Katherine M, McDonald Sarah D, Paré Guillaume, Atkinson Stephanie A, Teo Koon K, Meyre Dav |
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia. Journal of lipid research 2022 4 63 (6): 100209. Dong Weilai, Wong Karen H Y, Liu Youbin, Levy-Sakin Michal, Hung Wei-Chien, Li Mo, Li Boyang, Jin Sheng Chih, Choi Jungmin, Lopez-Giraldez Francesc, Vaka Dedeepya, Poon Annie, Chu Catherine, Lao Richard, Balamir Melek, Movsesyan Irina, Malloy Mary J, Zhao Hongyu, Kwok Pui-Yan, Kane John P, Lifton Richard P, Pullinger Clive |
Rare variants in previously identified linkage regions associated with carotid plaque in Dominican Republic families. PloS one 2022 1 17 (1): e0250799. Dueker Nicole D, Beecham Ashley, Wang Liyong, Dong Chuanhui, Sacco Ralph L, Blanton Susan H, Rundek Tatja |
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- Page last updated:May 13, 2024
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