✦ LIBER ✦

FIRST STUDY OF THE F508del MUTATION IN MALAYSIAN CHILDREN DIAGNOSED WITH CYSTIC FIBROSIS

✍ Scribed by Anna Marie Nathan

Book ID: 108956202
Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 83 KB
Volume: 47
Category: Article
ISSN: 1034-4810
DOI: 10.1111/j.1440-1754.2011.02149.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Growth in prepubertal children with cyst

Growth in prepubertal children with cystic fibrosis, homozygous for the ΔF508 mutation

✍ Bigna M. Keller; Carmen Casaulta Aebischer; Richard Kraemer; Martin H. Schöni 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 223 KB

Ivacaftor in Subjects With Cystic Fibros

Ivacaftor in Subjects With Cystic Fibrosis Who Are Homozygous for the F508del-CFTR Mutation

✍ Flume, Patrick A. 📂 Article 📅 2012 🏛 American College of Chest Physicians 🌐 English ⚖ 834 KB

Allele specific PCR with microfluorometr

Allele specific PCR with microfluorometry: application to the detection of del F508 mutation in cystic fibrosis

✍ Akihiro Yamaguchi; Juan Alberto Nepote; Maliheh Kadivar; Yasuko Tagami; Masaru F 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 170 KB

Population screening if F508del (ΔF508),

Population screening if F508del (ΔF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina

✍ María Roqué; Clara Pott Godoy; Mariana Castellanos; Eduardo Pusiol; Luis S. Mayo 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 35 KB

Cystic fibrosis (CF) is the most common autosomal recessive disease in the Caucasian population. The disease can be caused by one of the more than 900 different mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene. However, the deletion of the phe508-codon is the most pre

Effect of the F508del genotype on outcom

Effect of the F508del genotype on outcomes of endoscopic sinus surgery in children with cystic fibrosis

✍ Do, Bao Anh Julie; Lands, Larry C; Saint-Martin, Christine; Mascarella, Marco A; 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 294 KB

61* VX-770 in subjects with cystic fibro

61* VX-770 in subjects with cystic fibrosis who are homozygous for the F508del-CFTR mutation

✍ P.A. Flume; D.S. Borowitz; T.G. Liou; H. Li; K. Yen; C.L. Ordonez; D.E. Geller 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 45 KB