NDLI: Interaction Between Hb Hasharon and a-Thalassemia : An Approach to the Problem of the Number ofHuman a Loci

Content Provider	Semantic Scholar
Author	Pich, P. G. Saglio, Giuseppe Camaschella, Clara David, Onorata Vasino, Maria Ausilia Ciocca Ricco, Giuseppe Mazza, Umberto
Copyright Year	2005
Abstract	We report the case of an Italian infant girl hand, in the Askenazy carriers of Hb Hafrom Polesine (Po delta region in northern sharon, Hb Hasharon is probably linked to Italy) who was heterozygous for Hb Haa normal a gene. In comparing Hb Hasharon and a-thalassemia, did not synthesharon's behavior with that of other a size any normal HbA, and had 3% HbH on variants, particularly HbG Philadelphia, electrophoresis. Hematologic and biosynfrequent recombinations between a structhetic studies on Hb Hasharon carriers of tural genes were suggested. The possible the propositus' family suggest the possibilidentity between the single a locus and ity that the Hb Hasharon gene is linked to the a2-thalassemia genotype is disan a-thalassemia gene. On the other cussed.
File Format	PDF HTM / HTML
Alternate Webpage(s)	http://www.bloodjournal.org/content/bloodjournal/51/2/339.full.pdf?sso-checked=true
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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