Identification of CFTR variants in Latino patients with cystic fibrosis from the Dominican Republic and Puerto Rico-Reference-Cited by-同舟云学术

Identification of CFTR variants in Latino patients with cystic fibrosis from the Dominican Republic and Puerto Rico

Published:2019-10-30 Issue:2 Volume:55 Page:533-540
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol

Author:

Zeiger Andrew M.¹,McGarry Meghan E.²^ORCID,Mak Angel C. Y.¹,Medina Vivian³,Salazar Sandra¹,Eng Celeste¹,Liu Amy K.¹,Oh Sam S.¹,Nuckton Thomas J.¹,Jain Deepti⁴,Blackwell Thomas W.⁵,Kang Hyun Min⁵,Abecasis Goncalo⁵,Oñate Leandra Cordero⁶,Seibold Max A.⁷,Burchard Esteban G.¹⁸,Rodriguez‐Santana Jose³

Affiliation:

1. Department of MedicineUniversity of California San Francisco San Francisco California

2. Department of PediatricsUniversity of California San Francisco San Francisco California

3. Department of PediatricsCentro de Neumología Pediátrica San Juan Puerto Rico

4. Department of BiostatisticsUniversity of Washington Seattle Washington

5. Department of Biostatistics, Center for Statistical GeneticsUniversity of Michigan Ann Arbor Michigan

6. Department of PediatricsNeumología Pediátrica del Hospital Infantil Dr. Robert Reid Cabral Santo Domingo República Dominicana

7. Department of PediatricsNational Jewish Health Denver Colorado

8. Department of Bioengineering and Therapeutic SciencesUniversity of California San Francisco San Francisco California

Funder

National Institute of Environmental Health Sciences

Cystic Fibrosis Foundation Therapeutics

National Institute on Minority Health and Health Disparities

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.24549

Reference42 articles.

1. Pulmonary function disparities exist and persist in Hispanic patients with cystic fibrosis: A longitudinal analysis

2. Disparities in Mortality of Hispanic Patients with Cystic Fibrosis in the United States. A National and Regional Cohort Study

3. Hispanic Infants with Cystic Fibrosis Show Low CFTR Mutation Detection Rates in the Illinois Newborn Screening Program

4. The Spectrum of CFTR Variants in Nonwhite Cystic Fibrosis Patients

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