Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa

Publisher: John Wiley & Sons Inc

E-ISSN: 1741-4520|58|1|10-15

ISSN: 0914-3505

Source: CONGENITAL ANOMALIES, Vol.58, Iss.1, 2018-01, pp. : 10-15

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