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Novel locus for X linked recessive high myopia maps to Xq23–q25 but outside MYP1
BACKGROUND: High myopia is a common genetic variation in most cases, affecting 1–2% of people, and is the fourth most common disorder causing blindness worldwide. Six autosomal dominant loci and one X‐linked recessive locus have been reported, but no genes responsible for high myopia have been ident...
Tallennettuna:
| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Group
2006
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2564525/ https://ncbi.nlm.nih.gov/pubmed/16648373 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.037853 |
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