Identification of a Novel Heterozygous Missense Mutation in the CACNA1F Gene in a Chinese Family with Retinitis Pigmentosa by Next Generation Sequencing
Background. Retinitis pigmentosa (RP) is an inherited retinal degenerative disease, which is clinically and genetically heterogeneous, and the inheritance pattern is complex. In this study, we have intended to study the possible association of certain genes with X-linked RP (XLRP) in a Chinese famil...
Main Authors: | Qi Zhou, Jingliang Cheng, Weichan Yang, Mousumi Tania, Hui Wang, Md. Asaduzzaman Khan, Chengxia Duan, Li Zhu, Rui Chen, Hongbin Lv, Junjiang Fu |
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Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2015-01-01
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Series: | BioMed Research International |
Online Access: | http://dx.doi.org/10.1155/2015/907827 |
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