Gilbert's syndrome accounts for the phenotypic variability of congenital clyserythropoietic anemia type ii (cda-ii)

Journal of Pediatrics

Volumn 136, Issue 4, 2000, Pages 556-559

  Perrotta, Silverio ^a,b   Del Giudice, Emanuele Miraglia ^a,b   Carbone, Ruggiero ^a,b   Servedio, Veronica ^a,b   Schettini Jr , Federico ^a,b   Nobili, Bruno ^a,b   Iolascon, Achille ^a,b  

^a SECOND UNIVERSITY OF NAPLES   (Italy)

^b UNIVERSITY OF BARI   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN;

ADOLESCENT; ADULT; ARTICLE; BILIRUBIN BINDING; BILIRUBIN BLOOD LEVEL; CHILD; CLINICAL ARTICLE; DYSERYTHROPOIESIS; GALLSTONE FORMATION; GENETIC VARIABILITY; GILBERT DISEASE; HEREDITARY HEMOLYTIC ANEMIA; HUMAN; HYPERBILIRUBINEMIA; PHENOTYPE; PRIORITY JOURNAL;

EID: 0033943506     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(00)90026-X     Document Type: Article

References (11)

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8. 8. Alloisio N, Texier P, Denoroy L, Berger C, Miraglia del Giudice E, Perrotta S, et al. The cisternae decorating the red blood cell membrane in Congenital Dyserythropoietic Anemia (type II) originate from the endoplasmic reticulum. Blood 1996;87:4433-9.
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