A founder mutation in CERKL is a major cause of retinal dystrophy in Finland

Publisher: John Wiley & Sons Inc

E-ISSN: 1755-3768|96|2|183-191

ISSN: 1755-375X

Source: ACTA OPHTHALMOLOGICA, Vol.96, Iss.2, 2018-03, pp. : 183-191

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Abstract