Open AccessLoeys–Dietz syndrome is a specific phenotype and not a concomitant of any mutation in a gene involved in TGF-β signaling
Author(s) -
Reed E. Pyeritz,
Guillaume Jondeau,
Rocio Moran,
Julie De Backer,
Eloisa Arbustini,
Anne De Paepe,
Dianna M. Milewicz
Publication year - 2014
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1038/gim.2014.63
Subject(s) - phenotype , mutation , gene , genetics , concomitant , biology , transforming growth factor , medicine , bioinformatics , microbiology and biotechnology
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