1.
Lakartidningen
; 103(9): 657-60, 2006.
Article
in Swedish
| MEDLINE
| ID: mdl-16583542
Subject(s)
Glycogen Storage Disease Type VII/genetics , Hemolysis/genetics , Adult , Child , Female , Humans , Male , Muscle Fatigue/genetics , Mutation , Pedigree , Phosphofructokinase-1, Muscle Type/genetics , Sweden
2.
Lakartidningen
; 100(34): 2580-2, 2003 Aug 21.
Article
in Swedish
| MEDLINE
| ID: mdl-12968316
ABSTRACT
This report briefly reviews mutations known to cause beta-thalassemia in endogenous Swedish families. A unique mutation caused by a 12-bp deletion in exon 3 of the beta-globin gene has been found in four separate families originating from the island of Gotland in the Baltic.