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Anglický jazyk
Beta Thalassemia Mutations in Sudanese Patients
Autor: Rabab Hassan Elshaikh Mahmoud
Thalassemia is a"Mendelian autosomal recessive heritable blood disorder it's a group of genetically determined microcytic, hypochromic anemia's resulting from a decrease in synthesis of one or more globin chains in the hemoglobin moleculer Beta thalassemia... Viac o knihe
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O knihe
Thalassemia is a"Mendelian autosomal recessive heritable blood disorder it's a group of genetically determined microcytic, hypochromic anemia's resulting from a decrease in synthesis of one or more globin chains in the hemoglobin moleculer Beta thalassemia is a fairly common blood disorder worldwide. The parents of an affected child are obligate heterozygotes and carry a single copy of a disease-causing beta globin gene mutation. At conception, each child of heterozygotes parents has 25% chance of being affected, 50% chance of being an asymptomatic carrier, and 25% chance of being unaffected and not carrier.
- Vydavateľstvo: LAP LAMBERT Academic Publishing
- Rok vydania: 2019
- Formát: Paperback
- Rozmer: 220 x 150 mm
- Jazyk: Anglický jazyk
- ISBN: 9786200478399
