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Identification of a missense mutation in MIP gene via mutation analysis of a Guangxi Zhuang ethnic pedigree with congenital nuclear cataracts

At present, congenital cataract is the world's leading cause of blindness among children. The aim of the present study was to determine and analyze the genetic disorder associated with a congenital nuclear cataract in a three-generation family of Guangxi Zhuang ethnicity. A total of 3 affected...

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Bibliografski detalji
Izdano u:Exp Ther Med
Glavni autori: Zhou, Zhou, Li, Li, Lu, Lu, Min, Li
Format: Artigo
Jezik:Inglês
Izdano: D.A. Spandidos 2018
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6125844/
https://ncbi.nlm.nih.gov/pubmed/30214549
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2018.6557
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