Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa
Publication year
2018Source
Plos Genetics, 14, 8, (2018), pp. |, article e1007504ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Journal title
Plos Genetics
Volume
vol. 14
Issue
iss. 8
Page start
p. |
Page end
p. |
Subject
All institutes and research themes of the Radboud University Medical Center; Radboudumc 12: Sensory disorders DCMN: Donders Center for Medical NeuroscienceThis item appears in the following Collection(s)
- Academic publications [234237]
- Electronic publications [117187]
- Faculty of Medical Sciences [89178]
- Open Access publications [84231]
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