Protein Dysfunction in Human Genetic Disease

ISBN-13: 9781859960363 / Angielski / Twarda / 1997 / 272 str.

DM Swallow;YH Edwards;DM Swallow

Opis

This volume gives comprehensive coverage of human genetic disease mechanisms.

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

Recenzje

"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

Spis treści

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:

O autorze

Swallow\, DM; Edwards\, YH