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SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia
BACKGROUND: High myopia, with the characteristic feature of refractive error, is one of the leading causes of blindness worldwide. It has a high heritability, but only a few causative genes have been identified and the pathogenesis is still unclear. METHODS: We used whole genome linkage and exome se...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112430/ https://www.ncbi.nlm.nih.gov/pubmed/24891338 http://dx.doi.org/10.1136/jmedgenet-2014-102351 |