Novel intragenic deletions and point mutations of the ornithine transcarbamylase gene in congenital hyperammonemia
Patrick Calvas
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Laboratoire de Génétique, Université Paul Sabatier, Hǒpital Purpan, Place du Dr. Baylac, 31059 Toulouse Cedex, France
Search for more papers by this authorBertrand Ségues
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Search for more papers by this authorJean-Michel Rozet
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Search for more papers by this authorDaniel Rabier
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Search for more papers by this authorJean-Paul Bonnefond
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Search for more papers by this authorCorresponding Author
Arnold Munnich
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Unité de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 149, rue de Sèvres, 75743 Paris, FranceSearch for more papers by this authorPatrick Calvas
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Laboratoire de Génétique, Université Paul Sabatier, Hǒpital Purpan, Place du Dr. Baylac, 31059 Toulouse Cedex, France
Search for more papers by this authorBertrand Ségues
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Search for more papers by this authorJean-Michel Rozet
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Search for more papers by this authorDaniel Rabier
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Search for more papers by this authorJean-Paul Bonnefond
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Search for more papers by this authorCorresponding Author
Arnold Munnich
Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 75743 Paris-Cedex 15, France
Unité de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hǒpital des Enfants Malades, 149, rue de Sèvres, 75743 Paris, FranceSearch for more papers by this author
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