Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Pierre Mutantu"'
Autor:
Revital Shemer, Roger Wumba, Walter G. Wasser, Pierre Mutantu, Etty Kruzel-Davila, Nazaire M. Nseka, Justine B. Bukabau, Jeannine Luse, Nestor M Pakasa, Etienne Cavalier, Eric P. Cohen, Vieux M. Mokoli, Anat Reiner-Benaim, Ernest Kiswaya Sumaili, Jean Robert R. Makulo, Geoffrey Boner, Meyer Lifschitz, Karl Skorecki
Publikováno v:
Clinical Kidney Journal. 12:188-195
Background Sub-Saharan Africans exhibit a higher frequency of chronic kidney disease (CKD) than other populations. In this study, we sought to determine the frequency of apolipoprotein L1 (APOL1) genotypes in hypertension-attributed CKD in Kinshasa,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08f768e68b2d79cd880c89ef3c9d73ed
https://doi.org/10.1093/ckj/sfy073
https://doi.org/10.1093/ckj/sfy073
Autor:
Anniek Corveleyn, Papino Mukaba, Prosper Lukusa Tshilobo, Gerrye Mubungu, Pierre Mutantu, Gertrude Luyeye, Bruno-Paul Tady, Aimé Lumaka, Koenraad Devriendt
Publikováno v:
European Journal of Medical Genetics. 57:169-173
Apert syndrome (OMIM 101200 ) is a rare genetic condition characterized by craniosynostosis and syndactyly of hands and feet with clinical variability. Two single nucleotides mutations in the linker region between the immunoglobulin-like domains II a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae8d3ea0ef72ba85db762f1668c5fbc7
https://doi.org/10.1016/j.ejmg.2014.01.004
https://doi.org/10.1016/j.ejmg.2014.01.004