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1 Ergebnisse
1
CAMK2D De Novo Missense Variant in Patient with Syndromic N..:
Ekaterina R. Tolmacheva
;
Jekaterina Shubina
;
Taisiya O. Kochetkova
...
https://www.mdpi.com/2073-4425/14/6/1177. , 2023
Link:
https://doi.org/10.3390/genes14061177
RT Journal T1
CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:eef3764fe84640759b8b78b290ccd89c&Exemplar=1&LAN=DE A1 Ekaterina R. Tolmacheva A1 Jekaterina Shubina A1 Taisiya O. Kochetkova A1 Lubov' V. Ushakova A1 Ekaterina L. Bokerija A1 Grigory S. Vasiliev A1 Galina V. Mikhaylovskaya A1 Ekaterina E. Atapina A1 Nadezhda V. Zaretskaya A1 Gennady T. Sukhikh A1 Denis V. Rebrikov A1 Dmitriy Yu. Trofimov PB MDPI AG YR 2023 K1 dilated cardiomyopathy K1 neurodevelopmental disorder K1 whole exome sequencing K1 WES K1 trio K1 CAMK2D K1 Genetics K1 QH426-470 JF https://www.mdpi.com/2073-4425/14/6/1177 LK http://dx.doi.org/https://doi.org/10.3390/genes14061177 DO https://doi.org/10.3390/genes14061177 SF ELIB - SuUB Bremen
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