Highly Recurrent RET Mutations and Novel Mutations in Genes of the Receptor Tyrosine Kinase and Endothelin Receptor B Pathways in Chinese Patients with Sporadic Hirschsprung Disease

Clinical Chemistry

Volumn 50, Issue 1, 2004, Pages 93-100

  Garcia Barceló, Mercè ^a   Sham, Mai Har ^a   Lee, Wing Shan ^a   Lui, Vincent Chi Hang ^a   Chen, Benedict Ling Sze ^a   Wong, Kenneth Kak Yuen ^a   Wong, Joyce Suet Wan ^a   Tam, Paul Kwong Hang ^a  

^a UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

ENDOTHELIN 3; ENDOTHELIN B RECEPTOR; GLIAL CELL LINE DERIVED NEUROTROPHIC FACTOR; PROTEIN RET; PROTEIN TYROSINE KINASE;

ARTICLE; CHINESE; CONTROLLED STUDY; EXON; FEMALE; GENE AMPLIFICATION; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; GENETIC SCREENING; HIRSCHSPRUNG DISEASE; HUMAN; INTESTINE INNERVATION; INTRON; MAJOR CLINICAL STUDY; MALE; MUTATION RATE; POLYMERASE CHAIN REACTION; SIGNAL TRANSDUCTION; STATISTICAL SIGNIFICANCE;

ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; ENDOTHELIN-3; FEMALE; GENOTYPE; GERM-LINE MUTATION; GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR; HIRSCHSPRUNG DISEASE; HUMANS; MALE; MUTATION; NERVE GROWTH FACTORS; PHENOTYPE; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTORS, ENDOTHELIN; RECURRENCE; SIGNAL TRANSDUCTION;

EID: 1642574220     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1373/clinchem.2003.022061     Document Type: Article

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