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. 2003 Jul;40(7):e90.

doi: 10.1136/jmg.40.7.e90.

Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele

I Perrault¹, S Hanein, S Gerber, F Barbet, J-L Dufier, A Munnich, J-M Rozet, J Kaplan

Affiliations

PMID: 12843339
PMCID: PMC1735514
DOI: 10.1136/jmg.40.7.e90

Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele

I Perrault et al. J Med Genet. 2003 Jul.

. 2003 Jul;40(7):e90.

doi: 10.1136/jmg.40.7.e90.

Authors

I Perrault¹, S Hanein, S Gerber, F Barbet, J-L Dufier, A Munnich, J-M Rozet, J Kaplan

Affiliation

¹ Unité de Recherches sur les Handicaps Génétiques de l'Enfant, Hôpital Necker-Enfants Malades, 149 rue de Sévres, 75743 Paris Cedex 15, France.

PMID: 12843339
PMCID: PMC1735514
DOI: 10.1136/jmg.40.7.e90

No abstract available

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