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De novo missense mutations in the NAA10 gene cause severe n..:
Popp, Bernt
;
Støve, Svein I
;
Endele, Sabine
...
European Journal of Human Genetics. 23 (2014) 5 - p. 602-609 , 2014
Link:
https://doi.org/10.1038/ejhg.2014.150
RT Journal T1
De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_ejhg.2014.150&Exemplar=1&LAN=DE A1 Popp, Bernt A1 Støve, Svein I A1 Endele, Sabine A1 Myklebust, Line M A1 Hoyer, Juliane A1 Sticht, Heinrich A1 Azzarello-Burri, Silvia A1 Rauch, Anita A1 Arnesen, Thomas A1 Reis, André PB Springer Science and Business Media LLC YR 2014 SN 1018-4813 SN 1476-5438 JF European Journal of Human Genetics VO 23 IS 5 SP 602 OP 609 LK http://dx.doi.org/https://doi.org/10.1038/ejhg.2014.150 DO https://doi.org/10.1038/ejhg.2014.150 SF ELIB - SuUB Bremen
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