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PMID: 6254584 Published · ppublish English Journal Article

Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced by his) carriers.

Blood ·Vol. 56 ·No. 6 ·1980-12-00 ·Pages 1145-9

Giglioni B, Comi P, Taramelli R, Ottolenghi S, Ciocca-Vasino MA, Anè C, Cappellini MD, Gianni AM

Abstract

Restriction enzymes analysis of the DNA from two unrelated Italian families with Hb Hasharon, a variant Hb (alpha 47asp replaced by his) frequently occurring in the Polesine area in Italy, indicates that this variant is associated to an alpha globin gene deletion. The alpha Hash genotype most likely results from a mutation on an alpha thal2 genotype.

MeSH Terms
Asparagine Chromosome Deletion DNA Restriction Enzymes/genetics Genes Genetic Carrier Screening Globins/biosynthesis,genetics Hemoglobins, Abnormal/genetics Histidine Humans Italy Thalassemia/genetics
Chemicals
Hemoglobins, Abnormal Histidine Asparagine Globins DNA Restriction Enzymes
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Giglioni B
Comi P
Taramelli R
Ottolenghi S
Ciocca-Vasino M A
Anè C
Cappellini M D
Gianni A M
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1980-12-00
Pages
1145-9
Language
English
Region
United States
NLM ID
7603509
Subset
IM
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