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Ophthalmic Genetics Volume 38, 2017 - Issue 1: Festschrift Honoring Irene Hussels Maumenee
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Research Reports

Screening for SLC7A14 gene mutations in patients with autosomal recessive or sporadic retinitis pigmentosa

Masako SugaharaDepartment of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, JapanView further author information
,
Maho OishiDepartment of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, JapanView further author information
,
Akio OishiDepartment of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, JapanCorrespondence[email protected]
View further author information
,
Ken OginoDepartment of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, JapanView further author information
,
Satoshi MorookaDepartment of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, JapanView further author information
,
Norimoto GotohDepartment of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan;Center for Genomic Medicine, Kyoto University Graduate School of Medicine, Kyoto, JapanView further author information
,
Inyeop KangCenter for Genomic Medicine, Kyoto University Graduate School of Medicine, Kyoto, JapanView further author information
&
Nagahisa YoshimuraDepartment of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, JapanView further author information
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Pages 70-73 | Received 24 Jun 2015, Accepted 17 Dec 2015, Published online: 30 Mar 2016
Supplemental material

Table 1: List of primers used for multiplex ligation-dependent probe amplification analysis

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Related Research Data

Screening for SLC7A14 gene mutations in patients with autosomal recessive or sporadic retinitis pigmentosa
Source: Figshare
Screening for SLC7A14 gene mutations in patients with autosomal recessive or sporadic retinitis pigmentosa
Source: Figshare

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