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A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484291/ https://www.ncbi.nlm.nih.gov/pubmed/30892800 http://dx.doi.org/10.1111/jcmm.14278 |
| _version_ | 1783414094458519552 |
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| author | Cheng, Jingliang Fu, Jiewen Zhou, Qi Xiang, Xiaohong Wei, Chunli Yang, Lisha Fu, Shangyi Khan, Md. Asaduzzaman Lv, Hongbin Fu, Junjiang |
| author_facet | Cheng, Jingliang Fu, Jiewen Zhou, Qi Xiang, Xiaohong Wei, Chunli Yang, Lisha Fu, Shangyi Khan, Md. Asaduzzaman Lv, Hongbin Fu, Junjiang |
| author_sort | Cheng, Jingliang |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-6484291 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2019 |
| publisher | John Wiley and Sons Inc. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-64842912019-05-03 A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree Cheng, Jingliang Fu, Jiewen Zhou, Qi Xiang, Xiaohong Wei, Chunli Yang, Lisha Fu, Shangyi Khan, Md. Asaduzzaman Lv, Hongbin Fu, Junjiang J Cell Mol Med Short Communications John Wiley and Sons Inc. 2019-03-20 2019-05 /pmc/articles/PMC6484291/ /pubmed/30892800 http://dx.doi.org/10.1111/jcmm.14278 Text en © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Short Communications Cheng, Jingliang Fu, Jiewen Zhou, Qi Xiang, Xiaohong Wei, Chunli Yang, Lisha Fu, Shangyi Khan, Md. Asaduzzaman Lv, Hongbin Fu, Junjiang A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree |
| title | A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree |
| title_full | A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree |
| title_fullStr | A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree |
| title_full_unstemmed | A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree |
| title_short | A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree |
| title_sort | novel splicing mutation in the prph2 gene causes autosomal dominant retinitis pigmentosa in a chinese pedigree |
| topic | Short Communications |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6484291/ https://www.ncbi.nlm.nih.gov/pubmed/30892800 http://dx.doi.org/10.1111/jcmm.14278 |
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