Hirschsprung's disease: Genetic mutations in mice and men

Gut

Volumn 41, Issue 4, 1997, Pages 436-441

  Robertson, K ^a   Mason, I ^a   Hall, S ^b  

^a MEDICAL RESEARCH COUNCIL   (United Kingdom)

^b Department of Anatomy ^*

Author keywords

[No Author keywords available]

Indexed keywords

ENDOTHELIN 3; PROTEIN TYROSINE KINASE; RECEPTOR;

AGANGLIONOSIS; EXPERIMENTAL MODEL; FAMILIAL DISEASE; GENE MUTATION; HIRSCHSPRUNG DISEASE; HUMAN; INTESTINE INNERVATION; LETHAL MUTANT; MOUSE MUTANT; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; PRIORITY JOURNAL; REVIEW;

EID: 0030865887     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.41.4.436     Document Type: Review

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