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Updated: Oct 9, 2026

06:33
Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
Identification of a novel beta0-thalassemia mutation, codons 80/81 (-C), in an Iranian family
X Feleki1, H Najmabadi, R Karimi-Nejad
1The Cyprus Institute of Neurology and Genetics, Nicosia.
Hemoglobin
|February 24, 2001
Abstract
No abstract available in PubMed .
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