Absence of motilin gene mutations in infantile hypertrophic pyloric stenosis

Journal of Pediatric Surgery

Volumn 43, Issue 3, 2008, Pages 443-446

  Svenningsson, Anna ^a,b   Lagerstedt, Kristina ^a   Omrani, Mir Davood ^a   Nordenskjöld, Agneta ^a,b  

^a KAROLINSKA INSTITUTE   (Sweden)

^b KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Erythromycin; Infantile hypertrophic pyloric stenosis; Motilin; V15A polymorphism

Indexed keywords

AMINO ACID; DNA; MOTILIN; SIGNAL PEPTIDE;

AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE; HUMAN; HYPERTROPHIC PYLORUS STENOSIS; INFANCY; INFANT; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

CASE-CONTROL STUDIES; DIGESTIVE SYSTEM SURGICAL PROCEDURES; FEMALE; GASTROINTESTINAL MOTILITY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFANT; MALE; MOTILIN; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; PYLORIC STENOSIS, HYPERTROPHIC; REFERENCE VALUES; RISK ASSESSMENT; SENSITIVITY AND SPECIFICITY;

EID: 40749108540     PISSN: 00223468     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpedsurg.2007.10.006     Document Type: Article

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