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1 Ergebnisse
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Novel variants in the CLCN4 gene associated with syndromic ..:
Sinan Li
;
Wenxin Zhang
;
Piao Liang
...
https://www.frontiersin.org/articles/10.3389/fneur.2023.1096969/full. , 2023
Link:
https://doi.org/10.3389/fneur.2023.1096969
RT Journal T1 <Title>Novel variants in the CLCN4 gene associated with syndromic X-linked intellectual disability</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:8c0af9dfe3844114a6bce3df42ada219&Exemplar=1&LAN=DE A1 Sinan Li A1 Wenxin Zhang A1 Piao Liang A1 Min Zhu A1 Bixia Zheng A1 Wei Zhou A1 Chunli Wang A1 Xiaoke Zhao PB Frontiers Media S.A. YR 2023 K1 intellectual disability K1 MRXSRC K1 CLCN4 gene K1 missense variant K1 splice site variant K1 Neurology. Diseases of the nervous system K1 RC346-429 JF https://www.frontiersin.org/articles/10.3389/fneur.2023.1096969/full LK http://dx.doi.org/https://doi.org/10.3389/fneur.2023.1096969 DO https://doi.org/10.3389/fneur.2023.1096969 SF ELIB - SuUB Bremen
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