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Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele
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  1. Correspondence to:
 Dr J Kaplan, Unité de Recherches sur les Handicaps Génétiques de l’Enfant, Hôpital Necker-Enfants Malades, 149 rue de Sévres, 75743 Paris Cedex 15, France; 
 kaplan{at}necker.fr
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Citation

Perrault I, Hanein S, Gerber S, et al
Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele

Publication history

  • First published July 1, 2003.
Online issue publication 
July 01, 2003

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