Novel intragenic deletions and point mutations of the ornithine transcarbamylase gene in congenital hyperammonemia.

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Published in Hum Mutat on January 01, 1998

Authors

P Calvas1, B Ségues, J M Rozet, D Rabier, J P Bonnefond, A Munnich

Author Affiliations

1: Unite de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U393, Hôpital des Enfants Malades, Paris, France.

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