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1 Ergebnisse
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Loss-of-function variant in the LRR domain of SLITRK2 impli..:
Tayyaba Afsar
;
Hongxia Fu
;
Hammal Khan
...
https://www.frontiersin.org/articles/10.3389/fgene.2023.1308116/full. , 2024
Link:
https://doi.org/10.3389/fgene.2023.1308116
RT Journal T1 <Title>Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:2824b0791d5a4f9aa0d463705e6ae6d2&Exemplar=1&LAN=DE A1 Tayyaba Afsar A1 Hongxia Fu A1 Hammal Khan A1 Zain Ali A1 Zamrud Zehri A1 Gohar Zaman A1 Safdar Abbas A1 Arif Mahmood A1 Qamre Alam A1 Junjian Hu A1 Suhail Razak A1 Muhammad Umair PB Frontiers Media S.A. YR 2024 K1 neurodevelopmental disorders K1 SLITRK2 K1 whole-exome sequencing K1 novel mutation K1 developmental anomaly K1 nonsense mutation K1 Genetics K1 QH426-470 JF https://www.frontiersin.org/articles/10.3389/fgene.2023.1308116/full LK http://dx.doi.org/https://doi.org/10.3389/fgene.2023.1308116 DO https://doi.org/10.3389/fgene.2023.1308116 SF ELIB - SuUB Bremen
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