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Loeys–Dietz syndrome is a specific phenotype and not a concomitant of any mutation in a gene involved in TGF-β signaling

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Year: 2014
Type: article
Source: Genetics in Medicine
DOI: 10.1038/gim.2014.63
Authors: Reed Pyeritz, Guillaume Jondeau, Rocio Moran, Julie De Backer, Eloisa Arbustini, Anne De Paepe, Dianna Milewicz
Institutions: University of Pennsylvania, Inserm, Assistance Publique – Hôpitaux de Paris, Hôpital Bichat-Claude-Bernard, Cleveland Clinic, Ghent University, Policlinico San Matteo Fondazione, The University of Texas Health Science Center at Houston
Language: English

Topic: Connective tissue disorders research
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: bronze
OpenAlex ID: W2000806933
FWCI: 2.19
Cites: 7
Cited by: 20
Related to: 10
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