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X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia
PURPOSE: To identify genetic mutations in three families with early onset high myopia (eoHM) limited to female members. METHODS: Genomic DNA was collected from participating members of families XF1, XF2, and XF3. Genome-wide linkage scans were performed on the largest family (XF1). Whole exome seque...
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| Veröffentlicht in: | Mol Vis |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Molecular Vision
2016
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5082638/ https://ncbi.nlm.nih.gov/pubmed/27829781 |
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