Comprehensive analysis of NRG1 common and rare variants in hirschsprung patients

PLoS ONE

Volumn 7, Issue 5, 2012, Pages

  Luzón Toro, Berta ^a,b   Torroglosa, Ana ^a,b   Núñez Torres, Rocío ^a,b   Enguix Riego, María Valle ^a,b   Fernández, Raquel María ^a,b   de Agustín, Juan Carlos ^a   Antiñolo, Guillermo ^a,b   Borrego, Salud ^a,b  

^a HOSPITAL UNIVERSITARIO VIRGEN DEL ROCÍO   (Spain)

^b CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; BINDING SITE; CAUCASIAN; CHINESE; CONTROLLED STUDY; EPIGENETICS; FEMALE; GENE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HIRSCHSPRUNG DISEASE; HUMAN; INTESTINE INNERVATION; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; NERVE CELL; NONHUMAN; NRG1 GENE; NUCLEOTIDE SEQUENCE; PROTEIN MODIFICATION; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SITE DIRECTED MUTAGENESIS;

EID: 84871265043     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0036524     Document Type: Article

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