Loading…

One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain

Saved in:

Bibliographic Details
Published in:	Blood 1989-03, Vol.73 (4), p.1075-1077
Main Authors:	Fei, Y J, Stoming, T A, Kutlar, A, Huisman, T H, Stamatoyannopoulos, G
Format:	Article
Language:	English
Subjects:	Glutamates - genetics Glutamic Acid Humans Mutation Thalassemia - genetics
Citations:	Items that cite this one
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!