Severe Jaundice in a Patient with a Previously Undescribed Glucose-6-phosphate Dehydrogenase (G6PD) Mutation and Gilbert Syndrome-Reference-Cited by-同舟云学术

Severe Jaundice in a Patient with a Previously Undescribed Glucose-6-phosphate Dehydrogenase (G6PD) Mutation and Gilbert Syndrome

Published:2002-03 Issue:2 Volume:28 Page:104-107
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Beutler Ernest,Gelbart Terri,Miller William

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference23 articles.

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4. A new exon 10 glucose-6-phosphate dehydrogenase mutation (G6PD “Rehovot”) in a Jewish Ethiopian family, with variable phenotypes;Iancovici-Kidon;Blood Cells Mol. Dis.,2000

5. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism;Jablonska-Skwiecinska;Hum. Mutat.,1999

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