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Autor:
Karyn Megy, William C. Nichols, Chung K. Wendy, Jonathan Stephens, Nicholas W. Morrell, Christopher J. Penkett, Stefan Gräf, Tobias Tilly, Richard C. Trembath, Michael W. Pauciulo, Divya Pandya, Carrie L. Welch, Carmen M. Treacy, Allan Lawrie, Smitha Rajaram, Martin R. Wilkins, Yufeng Shen, Emilia M. Swietlik, Andrew J. Swift, Laura Southgate, Marcella Cogliano, Na Zhu, Heritable Pah, Katie A. Lutz, Daniel Greene, US Pah Biobank Enrolling Centers' Investigators, Jennifer M. Martin
BackgroundApproximately 25% of patients with pulmonary arterial hypertension (PAH) have been found to harbor rare mutations in disease-causing genes. To identify missing heritability in PAH we integrated deep phenotyping with whole-genome sequencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aefc2b08f58f6acceecbdbdf86411295
https://doi.org/10.1101/2019.12.11.871210
https://doi.org/10.1101/2019.12.11.871210