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2013 | 1 |
2017 | 1 |
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High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population.
Orphanet J Rare Dis. 2013 Feb 5;8:20. doi: 10.1186/1750-1172-8-20.
Orphanet J Rare Dis. 2013.
PMID: 23379534
Free PMC article.
Whole exome sequencing using Ion Proton system enables reliable genetic diagnosis of inherited retinal dystrophies.
Riera M, Navarro R, Ruiz-Nogales S, Méndez P, Burés-Jelstrup A, Corcóstegui B, Pomares E.
Riera M, et al.
Sci Rep. 2017 Feb 9;7:42078. doi: 10.1038/srep42078.
Sci Rep. 2017.
PMID: 28181551
Free PMC article.
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