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Refining the clinical phenotype associated with missense va..:
Tharreau, Mylène
;
Garde, Aurore
;
Marlin, Sandrine
...
American Journal of Medical Genetics Part A. 188 (2022) 5 - p. 1600-1606 , 2022
Link:
https://doi.org/10.1002/ajmg.a.62642
RT Journal T1 <Title>Refining the clinical phenotype associated with missense variants in exons 38 and 39 of KMT2D</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.62642&Exemplar=1&LAN=DE A1 Tharreau, Mylène A1 Garde, Aurore A1 Marlin, Sandrine A1 Morel, Godelieve A1 Ernest, Sylvain A1 Nambot, Sophie A1 Duffourd, Yannis A1 Ternoy, Ninon A1 Duvillard, Christian A1 Banka, Siddharth A1 Philippe, Christophe A1 Thauvin‐Robinet, Christel A1 Mau‐Them, Frederic Tran A1 Faivre, Laurence PB Wiley YR 2022 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 188 IS 5 SP 1600 OP 1606 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.62642 DO https://doi.org/10.1002/ajmg.a.62642 SF ELIB - SuUB Bremen
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