This is a summary of research advances which have implications for a number of diseases, including muscular dystrophy and cystic fibrosis. The text describes how these advances are leading to an understanding of the diseases' pathology, an essential first stage for devising treatment. The contributors also explain how knowledge gained through the discovery of various genes and associated mutations has enriched the wider field of genetics.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
A large proportion of human disease is caused by faulty genes, but until recently very few of these genes were known. Advances in molecular genetics over the last ten years have made it possible to systematically track down, isolate and begin to understand the function of these disease genes. This book describes the isolation of the genes responsible for a number of important human diseases, including Huntington′s disease, muscular dystrophy and cystic fibrosis.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : Plurabelle Books Ltd, Cambridge, Royaume-Uni
Hardcover. Etat : Good. Series: Molecular Medical Science 252p hardback, white laminated boards, from a Cambridge college library, clean tight copy Language: English. N° de réf. du vendeur 158335
Quantité disponible : 1 disponible(s)
Vendeur : Anybook.com, Lincoln, Royaume-Uni
Etat : Fair. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. Book contains pencil markings. In fair condition, suitable as a study copy. No dust jacket. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,600grams, ISBN:9780471934592. N° de réf. du vendeur 9807177
Quantité disponible : 1 disponible(s)