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Autor:
Mine Koprulu, Yajie Zhao, Eleanor Wheeler, Liang Dong, Nuno Rocha, Chen Li, John D Griffin, Satish Patel, Marcel Van de Streek, Craig A Glastonbury, Isobel D Stewart, Felix R Day, Jian’an Luan, Nicholas Bowker, Laura B L Wittemans, Nicola D Kerrison, Lina Cai, Debora M E Lucarelli, Inês Barroso, Mark I McCarthy, Robert A Scott, Vladimir Saudek, Kerrin S Small, Nicholas J Wareham, Robert K Semple, John R B Perry, Stephen O’Rahilly, Luca A Lotta, Claudia Langenberg, David B Savage
Publikováno v:
Koprulua, M, Zhaoa, Y, Wheeler, E, Liang, D, Rocha, N, Li, C, Griffin, J D, Patel, S, Van de Streek, M, Glastonbury, C A, Stewart, I, Day, F R, Luan, J, Bowker, N, Wittemans, L B L, Kerrison, N D, Cai, L, Lucarelli, D M E, Barroso, I, McCarthy, M I, Scott, R A, Saudek, V, Small, K S, Wareham, N J, Semple, R K, Perry, J R B, O’Rahilly, S, Lotta, L A, Langenberg, C & Savage, D B 2021, ' Identification of rare loss of function genetic variation regulating body fat distribution ', Journal of Clinical Endocrinology & Metabolism . https://doi.org/10.1210/clinem/dgab877
Context Biological and translational insights from large-scale, array-based genetic studies of fat distribution, a key determinant of metabolic health, have been limited by the difficulty in linking predominantly noncoding variants to specific gene t