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Exome sequencing links mutations in PARN and RTEL1 with f... | ResearchHub
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Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening
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Authors
Bridget Stuart
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Bridget Stuart
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Jungmin Choi
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•
Christine Garcia
Published
April 7, 2015
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Journal
Nature Genetics
Topics
Biology
Pathology
Medicine
Physiology
Internal Medicine
Show all topics
DOI
10.1038/ng.3278
