Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease

Human Molecular Genetics

Volumn 7, Issue 9, 1998, Pages 1449-1452

  Doray, Bérénice ^a   Salomon, Rémi ^a   Amiel, Jeanne ^a   Pelet, Anna ^a   Touraine, Renaud ^a   Billaud, Marc ^b   Attié, Tania ^a   Bachy, Bruno ^c   Munnich, Arnold ^a   Lyonnet, Stanislas ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b CENTRE DE RECHERCHE EN CANCÉROLOGIE DE LYON   (France)

^c UNIVERSITÉ DE ROUEN   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GLIAL CELL LINE DERIVED NEUROTROPHIC FACTOR; LIGAND; NEUROTROPHIC FACTOR;

ARTICLE; AUTONOMIC NERVOUS SYSTEM; CONTROLLED STUDY; DOMINANT GENE; GENE SEGREGATION; GLIA CELL; HIRSCHSPRUNG DISEASE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MULTIFACTORIAL INHERITANCE; MYENTERIC PLEXUS; PEDIGREE; PENETRANCE; PRIORITY JOURNAL; PROTO ONCOGENE;

AMINO ACID SEQUENCE; BASE SEQUENCE; DNA; DNA PRIMERS; DROSOPHILA PROTEINS; FEMALE; GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR; GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR RECEPTORS; HETEROZYGOTE; HIRSCHSPRUNG DISEASE; HUMANS; LIGANDS; MALE; MUTATION; NERVE GROWTH FACTORS; NERVE TISSUE PROTEINS; NEURTURIN; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTO-ONCOGENE PROTEINS; PROTO-ONCOGENE PROTEINS C-RET; RECEPTOR PROTEIN-TYROSINE KINASES;

EID: 7344244286     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.9.1449     Document Type: Article

References (26)

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