Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): the ClinGen IEM Working Group and the phenylalanine hydroxylase gene
by Zastrow, Diane B. (Author)
, Baudet, Heather (Author)
, Shen, Wei (Author)
, Thomas, Amanda (Author)
, Si, Yue (Author)
, Weaver, Meredith A. (Author)
, Lager, Angela M. (Author)
, Liu, Jixia (Author)
, Mangels, Rachel (Author)
, Dwight, Selina S. (Author)
, Wright, Matt W. (Author)
, Dobrowolski, Steven F. (Author)
, Eilbeck, Karen (Author)
, Enns, Gregory M. (Author)
, Feigenbaum, Annette (Author)
, Lichter‐Konecki, Uta (Author)
, Lyon, Elaine (Author)
, Pasquali, Marzia (Author)
, Watson, Michael (Author)
, Blau, Nenad (Author)
, Steiner, Robert D. (Author)
, Craigen, William J. (Author)
, Mao, Rong (Author)
,
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