Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3
Kerrison, J B, Arnould, V J, Ferraz Sallum, J M, Vagefi, M R, Barmada, M M, Li, Y, Zhu, D, Maumenee, I H
Published in Archives of ophthalmology (1960) (01.06.1999)
Published in Archives of ophthalmology (1960) (01.06.1999)
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Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies
Devuyst, Olivier, Arnould, Véronique J.
Published in Nephrology, dialysis, transplantation (01.05.2008)
Published in Nephrology, dialysis, transplantation (01.05.2008)
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