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
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
More info about Taylor & Francis e-books