ZEB2, a new candidate gene for asplenia

Orphanet Journal of Rare Diseases

Volumn 9, Issue 1, 2014, Pages

  Pons, Linda ^a   Dupuis Girod, Sophie ^a   Cordier, Marie Pierre ^a   Edery, Patrick ^a,b   Rossi, Massimiliano ^a,b  

^a HOSPICES CIVILS DE LYON   (France)

^b LYON NEUROSCIENCE RESEARCH CENTER   (France)

Author keywords

Asplenia; Mowat Wilson syndrome; ZEB2

Indexed keywords

ARTICLE; ASPLENIA; CHILD; CHOANA ATRESIA; CLINICAL ARTICLE; CLUBFOOT; CORPUS CALLOSUM AGENESIS; DEVELOPMENTAL DISORDER; EPILEPSY; FEMALE; FULMINATING PURPURA; GENE; GENE MUTATION; HEART ATRIUM SEPTUM DEFECT; HEART VENTRICLE SEPTUM DEFECT; HETEROZYGOTE; HUMAN; INFANT; INFECTIOUS COMPLICATION; INTRACRANIAL HYPERTENSION; MICROCEPHALY; NEWBORN; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PNEUMOCOCCAL INFECTION; PRESCHOOL CHILD; SHORT STATURE; STRABISMUS; VESICOURETERAL REFLUX; WILSON DISEASE; ZEB2 GENE;

FACIES; FEMALE; HETEROTAXY SYNDROME; HIRSCHSPRUNG DISEASE; HOMEODOMAIN PROTEINS; HUMANS; INTELLECTUAL DISABILITY; MICROCEPHALY; REPRESSOR PROTEINS;

EID: 84892150410     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-9-2     Document Type: Article

References (11)

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