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Protein Dysfunction in Human Genetic Disease [Kõva köide]

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  • Formaat: Hardback, 272 pages, kõrgus x laius: 241x161 mm, kaal: 635 g
  • Ilmumisaeg: 15-Jun-1997
  • Kirjastus: Bios Scientific Publishers Ltd
  • ISBN-10: 1859960367
  • ISBN-13: 9781859960363
Teised raamatud teemal:
  • Formaat: Hardback, 272 pages, kõrgus x laius: 241x161 mm, kaal: 635 g
  • Ilmumisaeg: 15-Jun-1997
  • Kirjastus: Bios Scientific Publishers Ltd
  • ISBN-10: 1859960367
  • ISBN-13: 9781859960363
Teised raamatud teemal:
Recent years have seen rapid advances in our understanding of genetic diseases in terms of their molecular origins. In almost all cases where disease genes have been cloned, the mutations in the DNA sequence which are responsible for the clinical phenoty

Arvustused

"There are excellent chapters on many other disorders arising from dysfunctional proteins, which are all good descriptors of molecular and cellular mechanisms of disease." ; "Anyone interested in biology or human medicine would greatly benefit from readi

Mutation and Protein Dysfunction; Haemoglobin: Glucose 6-phosphate Dehydrogenase; Glycogen Storage disease due to Phosphorylase Kinase Deficiency; The Retinoblastoma Tumour Suppressor Protein and Cancer; Rhodopsin Mutations in Photoreceptor Degeneration:
Swallow\, DM; Edwards\, YH