Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype–Phenotype Correlations

Publisher： John Wiley & Sons Inc

E-ISSN： 1098-1004|34|11|1537-1546

ISSN： 1059-7794

Source： HUMAN MUTATION, Vol.34, Iss.11, 2013-11, pp. : 1537-1546

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