Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency.

Miraglia del Giudice, E

Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency. [electronic resource] - British journal of haematology May 1998 - 251-4 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0007-1048

10.1046/j.1365-2141.1998.00688.x doi


Child
Child, Preschool
Female
Gene Expression
Heterozygote
Humans
Infant
Male
Mutation
Pedigree
Polymorphism, Genetic
RNA, Messenger--metabolism
Spectrin--deficiency
Spherocytosis, Hereditary--genetics