Hemoglobin variants: Difference between revisions
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'''Hemoglobin variants''' are mutant forms of [[hemoglobin]] in a [[population]] (usually of humans), caused by variations in genetics. Some well-known hemoglobin variants such as [[sickle-cell anemia]] are responsible for diseases, and are considered hemoglobinopathies. Other variants cause no detectable [[pathology]], and are thus considered non-pathological variants. | '''Hemoglobin variants''' are mutant forms of [[hemoglobin]] in a [[population]] (usually of humans), caused by variations in genetics. Some well-known hemoglobin variants such as [[sickle-cell anemia]] are responsible for diseases, and are considered hemoglobinopathies. Other variants cause no detectable [[pathology]], and are thus considered non-pathological variants. | ||
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Latest revision as of 15:53, 9 August 2012
Hemoglobin variants are mutant forms of hemoglobin in a population (usually of humans), caused by variations in genetics. Some well-known hemoglobin variants such as sickle-cell anemia are responsible for diseases, and are considered hemoglobinopathies. Other variants cause no detectable pathology, and are thus considered non-pathological variants.
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