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Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness
PURPOSE: This study was undertaken to investigate the causal mutations responsible for autosomal recessive congenital stationary night blindness (CSNB) in consanguineous Pakistani families. METHODS: Two consanguineous families with multiple individuals manifesting symptoms of stationary night blindn...
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| 發表在: | Mol Vis |
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| Main Authors: | , , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Molecular Vision
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4636350/ https://ncbi.nlm.nih.gov/pubmed/26628857 |
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