학술논문

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
kinase, endopeptidase and other proteins of small size
Document Type
Report
Author
Braun, Daniela ARao, JiaMollet, GeraldineSchapiro, DavidDaugeron, Marie-ClaireTan, WeizhenGribouval, OlivierBoyer, OliviaRevy, PatrickJobst-Schwan, TilmanSchmidt, Johanna MagdalenaLawson, Jennifer ASchanze, DennyAshraf, ShaziaUllmann, Jeremy F PHoogstraten, Charlotte ABoddaert, NathalieCollinet, BrunoMartin, GaëlleLiger, DominiqueLovric, SvjetlanaFurlano, MonicaGuerrera, I ChiaraSanchez-Ferras, OralyHu, Jennifer FBoschat, Anne-ClaireSanquer, SylviaMenten, BjörnVergult, SarahDe Rocker, NinaAirik, MerlinHermle, TobiasShril, ShirleeWidmeier, EugenGee, Heon YungChoi, Won-IlSadowski, Carolin EPabst, Werner LWarejko, Jillian KDaga, AnkanaBasta, TamaraMatejas, VerenaScharmann, KarinKienast, Sandra DBehnam, BabakBeeson, BrendanBegtrup, AmberBruce, MalcolmCh'ng, Gaik-SiewLin, Shuan-PeiChang, Jui-HsingChen, Chao-HueiCho, Megan TGaffney, Patrick MGipson, Patrick EHsu, Chyong-HsinKari, Jameela AKe, Yu-YuanKiraly-Borri, CathyLai, Wai-mingLemyre, EmmanuelleLittlejohn, Rebecca OkashahMasri, AmiraMoghtaderi, MastanehNakamura, KazuyukiOzaltin, FatihPraet, MarleenPrasad, ChitraPrytula, AgnieszkaRoeder, Elizabeth RRump, PatrickSchnur, Rhonda EShiihara, TakashiSinha, Manish DSoliman, Neveen ASoulami, KenzaSweetser, David ATsai, Wen-HuiTsai, Jeng-DawTopaloglu, RezanVester, UdoViskochil, David HVatanavicharn, NithiwatWaxler, Jessica LWierenga, Klaas JWolf, Matthias T FWong, Sik-NinLeidel, Sebastian ATruglio, GessicaDedon, Peter CPoduri, AnnapurnaMane, ShrikantLifton, Richard PBouchard, MaximeKannu, PeterChitayat, DavidMagen, DaniellaCallewaert, Bertvan Tilbeurgh, HermanZenker, MartinAntignac, CorinneHildebrandt, Friedhelm
Source
Nature Genetics. October 2017, Vol. 49 Issue 10, p1529, 10 p.
Subject
Development and progression
Genetic aspects
Health aspects
Nephrotic syndrome -- Genetic aspects -- Development and progression
Microcephaly -- Genetic aspects -- Development and progression
Gene mutation -- Health aspects
Genetic disorders -- Development and progression
Language
English
ISSN
1061-4036
Abstract
Author(s): Daniela A Braun [1]; Jia Rao [1]; Geraldine Mollet [2, 3]; David Schapiro [1]; Marie-Claire Daugeron [4]; Weizhen Tan [1]; Olivier Gribouval [2, 3]; Olivia Boyer [2, 3, 5]; [...]