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1 Ergebnisse
1
Novel Homozygous Missense Variant in Connexin Domain Causin..:
Hassan, Abdullah Y
;
Yousaf, Sairah
;
Levin, Moran R
...
International Journal of Molecular Sciences. , 2021
Link:
http://hdl.handle.net/10713/17512
RT Journal T1
Novel Homozygous Missense Variant in Connexin Domain Causing Congenital Nuclear and Cortical Cataracts
UL https://suche.suub.uni-bremen.de/peid=base-ftumarylandhshsl:oai:archive.hshsl.umaryland.edu:10713_17512&Exemplar=1&LAN=DE A1 Hassan, Abdullah Y A1 Yousaf, Sairah A1 Levin, Moran R A1 Saeedi, Osamah J A1 Riazuddin, Saima A1 Alexander, Janet L A1 Ahmed, Zubair M PB MDPI AG YR 2021 K1 African American K1 GJA3 K1 congenital cataract K1 cortical cataract K1 exome sequencing K1 nuclear cataract JF International Journal of Molecular Sciences LK http://hdl.handle.net/10713/17512 DO http://hdl.handle.net/10713/17512 SF ELIB - SuUB Bremen
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