Stock image for illustration purposes only - book cover, edition or condition may vary.
Cystic Fibrosis
Richard B. Moss
€ 123.78
FREE Delivery in Ireland
Description for Cystic Fibrosis
Paperback. Series: Allergy and Immunology. Num Pages: 262 pages, 20 black & white illustrations, biography. BIC Classification: MJCM1. Category: (P) Professional & Vocational. Dimension: 254 x 178 x 14. Weight in Grams: 515.
This work is concerned with Cystic Fibrosis (CF), the most common fatal genetic disease in the Caucasian population. The decade of the 1980s was one of spectacular progress in understanding the genetic and molecu lar basis of CF. The research breakthroughs of the decade began with the first fundamental insights, published in 1981-1983, into the basic cellular pathophysiology of CF with demonstrations of altered ion transport in spe cialized exocrine epithelial tissues (1-3). Research progress shifted into a triumph of "reverse genetics," using restriction-fragment-Iength polymor phism DNA technology (4), with the localization of the CF gene to a region of ... Read more
This work is concerned with Cystic Fibrosis (CF), the most common fatal genetic disease in the Caucasian population. The decade of the 1980s was one of spectacular progress in understanding the genetic and molecu lar basis of CF. The research breakthroughs of the decade began with the first fundamental insights, published in 1981-1983, into the basic cellular pathophysiology of CF with demonstrations of altered ion transport in spe cialized exocrine epithelial tissues (1-3). Research progress shifted into a triumph of "reverse genetics," using restriction-fragment-Iength polymor phism DNA technology (4), with the localization of the CF gene to a region of ... Read more
Product Details
Format
Paperback
Publication date
2013
Publisher
Humana Press Inc. United States
Number of pages
262
Condition
New
Series
Allergy and Immunology
Number of Pages
251
Place of Publication
Totowa, NJ, United States
ISBN
9781461267782
SKU
V9781461267782
Shipping Time
Usually ships in 15 to 20 working days
Ref
99-15
Reviews for Cystic Fibrosis