[Carrier frequency of alpha thalassemia mutations among newborns in northern Iran]
Journal of Gorgan University of Medical Sciences. 2016; 17 (4): 106-111
in Persian
| IMEMR
| ID: emr-177321
ABSTRACT
Background and Objective:
Alpha Thalassemia is one of the most prevalent hemaglobinophaties worldwide. Alpha thalasseima patients may represent wide spectrum of symptoms ranging from asymptomatic to severe life threatening anemia. This study was done to assess the carrier frequency of alpha globin gene mutations among newborns in north of Iran
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Index:
IMEMR (Eastern Mediterranean)
Language:
Persian
Journal:
J. Gorgan Univ. Med. Sci.
Year:
2016
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