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New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy
PURPOSE: The mutations responsible for Best vitelliform macular dystrophy (BVMD) are found in a gene called VMD2. The VMD2 gene encodes a transmembrane protein named bestrophin‐1 (hBest1) which is a Ca(2+)‐sensitive chloride channel. This study was performed to identify disease‐specific mutations in...
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| Main Authors: | , , , , , , , , , , , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BMJ Group
2007
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2598027/ https://ncbi.nlm.nih.gov/pubmed/17287362 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.044511 |
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