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Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families
Aims: To describe the clinical phenotype of X linked juvenile retinoschisis in eight Italian families with six different mutations in the XLRS1 gene. Methods: Complete ophthalmic examinations, electroretinography and A and B-scan standardised echography were performed in 18 affected males. The codin...
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| Autori principali: | , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Copyright 2003 British Journal of Ophthalmology
2003
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1771850/ https://ncbi.nlm.nih.gov/pubmed/12928282 |
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