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Dallapiccola B, Chessa L, Vignetti P, Ferrante E, Gandini E (1979) Increased HK-1 activity levels in the red cells of a patient with a de novo trisomy 10p:t(Y;10)(p12;p12). Hum Genet 50:45–49
Dallapiccola B, Lungarotti MS, Magnani M, Dachà M (1981) Evidence of gene dosage effect for HK-1 in the red cells of a patient with trisomy 10pter-p13. Ann Génét (Paris), 24:45–47
Gitelman BJ, Simpson NE (1982) Regional mapping of the locus for hexokinase-1 (HK1) to 10p11-q23 by gene dosage in human fibroblasts. Hum Genet 60:227–229
Magnani M, Stocchi V, Piatti E, Dachà M, Dallapiccola B, Fornaini G (to be published) Red blood cell glucose metabolism in trisomy 10p. Possible role of hexokinase in the erythrocyte
Stocchi V, Magnani M, Canestrari F, DachàM, Fornaini G (1982) Multiple forms of human red blood cell hexokinase. Preparation, characterization and age dependence. J Biol Chem. 257:2357–2364
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Magnani, M., Dallapiccola, B. Regional mapping of the locus for hexokinase-1 (HK1). Hum Genet 62, 181 (1982). https://doi.org/10.1007/BF00282313
- Internal Medicine
- Metabolic Disease
- Regional Mapping