Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening - Concepedia

Concepedia

Publication | Open Access

Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening

DOI Full Paper Access

455

Citations

38

References

2015

Year

Bridget Stuart, Jungmin Choi, Samir Zaidi, Chao Xing, Brody Holohan, Rui Chen, Mihwa Choi, Pooja Dharwadkar, Fernando Torres, C Girod,

Nature Genetics

Mendelian DisorderLinks MutationsGenetic DisorderGeneticsPathologyPulmonary FibrosisMolecular GeneticsDisease Gene IdentificationFamilial Pulmonary FibrosisMedicineVariant Interpretation

References

	Year	Citations

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