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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...
में बचाया:
| में प्रकाशित: | Mol Vis |
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| मुख्य लेखकों: | , , , , , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Molecular Vision
2015
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4636350/ https://ncbi.nlm.nih.gov/pubmed/26628857 |
| टैग : |
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