Severity of oro-dental anomalies in Loeys-Dietz syndrome segregates by gene mutation

Background Loeys-Dietz syndrome (LDS), an autosomal dominant rare connective tissue disorder, has multisystemic manifestations, characterised by vascular tortuosity, aneurysms and craniofacial manifestations. Based on the associated gene mutations along the transforming growth factor-beta (TGF-β) pa...

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Detalles Bibliográficos
Autores principales: Jani, Priyam, Nguyen, Quynh C, Almpani, Konstantinia, Keyvanfar, Cyrus, Mishra, Rashmi, Liberton, Denise, Orzechowski, Pamela, Frischmeyer-Guerrerio, Pamela A, Duverger, Olivier, Lee, Janice S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Developmental Defects
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525783/
https://www.ncbi.nlm.nih.gov/pubmed/32152251
http://dx.doi.org/10.1136/jmedgenet-2019-106678

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525783/
https://www.ncbi.nlm.nih.gov/pubmed/32152251
http://dx.doi.org/10.1136/jmedgenet-2019-106678

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