Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five novel mutations (W1098C, 846delT, P750L, 4160insGGGG and 297-1G→A)-Reference-Cited by-同舟云学术

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Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five novel mutations (W1098C, 846delT, P750L, 4160insGGGG and 297-1G→A)

Published:2000-03-30 Issue:3 Volume:106 Page:360-365
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Orozco L.,Velázquez R.,Zielenski J.,Tsui L.-C.,Chávez M.,Lezana J.L.,Saldaña Y.,Hernández E.,Carnevale A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A personalized medicine approach to optimize care for a pediatric cystic fibrosis patient with atypical clinical symptoms;Pediatric Pulmonology;2023-10-11

3. Molecular Diagnostics of Cystic Fibrosis in Serbia: Our Approach to Meet the Diagnostic Challenges;Genetic Testing and Molecular Biomarkers;2020-04-01

4. Next-generation sequencing for identifying a novel/de novo pathogenic variant in a Mexican patient with cystic fibrosis: a case report;BMC Medical Genomics;2019-05-22

5. Incidencia de la fibrosis quística en Paraguay;Pediatría (Asunción);2019-04-24

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