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1 Ergebnisse
1
Novel Loss-of-Function Mutations in NPR2 Cause Acromesomeli..:
Jing Wu
;
Mengru Wang
;
Zhouyang Jiao
...
https://www.frontiersin.org/articles/10.3389/fgene.2022.823861/full. , 2022
Link:
https://doi.org/10.3389/fgene.2022.823861
RT Journal T1 <Title>Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:e763f90f540e45c9a8c685f8a3e18ed5&Exemplar=1&LAN=DE A1 Jing Wu A1 Mengru Wang A1 Zhouyang Jiao A1 Binghua Dou A1 Bo Li A1 Jianjiang Zhang A1 Haohao Zhang A1 Yue Sun A1 Xin Tu A1 Xiangdong Kong A1 Ying Bai PB Frontiers Media S.A. YR 2022 K1 acromesomelic dysplasia K1 maroteaux type K1 natriuretic peptide receptor 2 K1 loss-of-function mutation K1 growth hormone therapy K1 genotype analysis K1 Genetics K1 QH426-470 JF https://www.frontiersin.org/articles/10.3389/fgene.2022.823861/full LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.823861 DO https://doi.org/10.3389/fgene.2022.823861 SF ELIB - SuUB Bremen
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