z-logo
open-access-imgOpen Access
Small-scale high-throughput sequencing–based identification of new therapeutic tools in cystic fibrosis
Author(s) -
Jennifer Bonini,
Jessica Varilh,
Caroline Raynal,
C. Thèze,
Emmanuelle Beyne,
MariePierre Audrézet,
Claude Férec,
Thierry Bienvenu,
E. Girodon,
Sylvie TufferyGiraud,
Marie des Georges,
Mireille Claustres,
Magali TaulanCadars
Publication year - 2015
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1038/gim.2014.194
Subject(s) - cystic fibrosis , identification (biology) , throughput , computational biology , dna sequencing , scale (ratio) , medicine , computer science , biology , genetics , dna , geography , telecommunications , botany , cartography , wireless
Although 97-99% of CFTR mutations have been identified, great efforts must be made to detect yet-unidentified mutations.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom