## Defects of ␣ spectrin have been identified in many cases of hereditary elliptocytosis (HE) and hereditary pyropoikilocytosis (HPP). To aid in the genetic analysis of families with these disorders, the locations of three ␣-spectrin gene polymorphisms were mapped, the genetic basis of these polymo
Quantitative assessment of the association of the α-I fragment of spectrin with oligomers of intact spectrin
✍ Scribed by Nerida Cole; Gregory B. Ralston
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 553 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0020-711X
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