North Carolina newborn exome sequencing for universal screening (NC nexus) detects molecular etiologies underlying inborn errors of metabolism and hearing loss
Year: 2019
Type: article
Authors: Sanjeet Roy, Alicia Brandt, Chelsea Gustafson, Natasha T. Strande, Bryce A. Seifert, Lori Ramkissoon, A. Arreola, Claire Edgerly, Daniela M. DeCristo, Laura V. Milko, Phillips Owen, M. Li, Mai Xiong, Julianne O’Daniel, Megan A. Lewis, Ryan S. Paquin, Katherine J. Souris, Rita M. Butterfield, Donald B. Bailey, Christine Rini, Jessica K. Booker, Bradford C. Powell, Karen E. Weck, Caldwell Powell, Jonathan S. Berg, K. Lee, Ann Katherine M. Foreman, Myra I. Roche, Stephanie B. Crowley, Tamara S. Roman
Language: English
Subfield: Clinical Biochemistry
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2996945855