Wilson disease in offspring of affected patients: Report of four French families

Clinics and Research in Hepatology and Gastroenterology

Volumn 37, Issue 3, 2013, Pages 240-245

  Dufernez, Fabienne ^a,c   Lachaux, Alain ^b,c   Chappuis, Philippe ^c   De Lumley, Lionel ^d   Bost, Muriel ^c,e   Woimant, France ^c   Misrahi, Micheline ^a,c   Debray, Dominique ^a,c  

^a BICÊTRE HOSPITAL   (France)

^b HOSPICES CIVILS DE LYON   (France)

^c HÔPITAL LARIBOISIÈRE   (France)

^d DUPUYTREN UNIVERSITY HOSPITAL   (France)

^e Centre de Biologie et Pathologie Est   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; CERULOPLASMIN; COPPER; PENICILLAMINE; WILSON DISEASE PROTEIN;

ADOLESCENT; ADULT; AMINOTRANSFERASE BLOOD LEVEL; ARTICLE; BILIRUBIN BLOOD LEVEL; CERULOPLASMIN BLOOD LEVEL; CHRONIC GRAFT REJECTION; CLINICAL ARTICLE; CONSANGUINITY; COPPER METABOLISM; DNA SEQUENCE; DYSARTHRIA; DYSPHONIA; DYSTONIA; FAMILIAL DISEASE; FEMALE; FRAMESHIFT MUTATION; FRANCE; FULMINANT HEPATIC FAILURE; GAIT DISORDER; GENE MUTATION; GENE SEQUENCE; GENETIC COUNSELING; HAPLOTYPE; HEMOLYTIC ANEMIA; HETEROZYGOTE; HUMAN; LEARNING DISORDER; LEUKOPENIA; LIVER CIRRHOSIS; LIVER DISEASE; LIVER FUNCTION TEST; LIVER TRANSPLANTATION; MALE; MEDICAL HISTORY; MICROSATELLITE MARKER; MOLECULAR DIAGNOSIS; MUTATIONAL ANALYSIS; NEUROLOGIC DISEASE; PARENT; PHYSICAL EXAMINATION; PREGNANCY; PROGENY; SCREENING; SLIT LAMP; THROMBOCYTOPENIA; TISSUE INJURY; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; ADOLESCENT; ADULT; CATION TRANSPORT PROTEINS; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; FRANCE; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; HAPLOTYPES; HEPATOLENTICULAR DEGENERATION; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; MUTATION; PEDIGREE;

EID: 84878911497     PISSN: 22107401     EISSN: 2210741X     Source Type: Journal    
DOI: 10.1016/j.clinre.2013.01.001     Document Type: Article

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