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1 Ergebnisse
1
A novel mutation in RS1 and clinical manifestations in a Ch..:
Xiao-Fang Wang
;
Fei-Fei Chen
;
Xin Zhou
..
https://www.frontiersin.org/articles/10.3389/fgene.2022.993157/full. , 2022
Link:
https://doi.org/10.3389/fgene.2022.993157
RT Journal T1
A novel mutation in RS1 and clinical manifestations in a Chinese twin family with congenital retinoschisis
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:7bba7ab069704e34beee3129ade22268&Exemplar=1&LAN=DE A1 Xiao-Fang Wang A1 Fei-Fei Chen A1 Xin Zhou A1 Xin-Xuan Cheng A1 Zheng-Gao Xie PB Frontiers Media S.A. YR 2022 K1 congenital retinoschisis K1 gene mutation K1 RS1 K1 sequencing K1 genotype–phenotype K1 Genetics K1 QH426-470 JF https://www.frontiersin.org/articles/10.3389/fgene.2022.993157/full LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.993157 DO https://doi.org/10.3389/fgene.2022.993157 SF ELIB - SuUB Bremen
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