A novel mutation of MIP in a Chinese family with congenital nuclear cataract identified by whole-exome sequencing. (2nd January 2018)

Record Type:: Journal Article
Title:: A novel mutation of MIP in a Chinese family with congenital nuclear cataract identified by whole-exome sequencing. (2nd January 2018)
Main Title:: A novel mutation of MIP in a Chinese family with congenital nuclear cataract identified by whole-exome sequencing
Authors:: Liu, Shuaimei
Zhu, Peiran
Ni, Mengxia
Zhang, Mingchao
Jiang, Weijun
Yu, Maomao
Zhang, Jing
Wu, Qiuyue
Li, Weiwei
Xue, Chunyan
Xia, Xinyi
Abstract:
Is Part Of:: Ophthalmic genetics. Volume 39:Number 1(2018)
Journal:: Ophthalmic genetics
Issue:: Volume 39:Number 1(2018)
Issue Display:: Volume 39, Issue 1 (2018)
Year:: 2018
Volume:: 39
Issue:: 1
Issue Sort Value:: 2018-0039-0001-0000
Page Start:: 139
Page End:: 140
Publication Date:: 2018-01-02
Subjects:: Eye -- Diseases -- Genetic aspects -- Periodicals
Eye Diseases -- genetics -- Periodicals
Eye Diseases -- in infancy & childhood -- Periodicals
617.7
Journal URLs:: http://informahealthcare.com/loi/opg ↗
http://informahealthcare.com ↗
http://www.tandf.co.uk/journals/titles/13816810.asp ↗
DOI:: 10.1080/13816810.2017.1342133 ↗
Languages:: English
ISSNs:: 1381-6810
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 6270.893000
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Ingest File:: 5529.xml