Crossmark

Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis

Crossref DOI link: https://doi.org/10.1038/s41436-018-0300-5

Published Print: 2019-05

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Schrauwen, Isabelle

Valgaeren, Hanne

Tomas-Roca, Laura

Sommen, Manou

Altunoglu, Umut

Wesdorp, Mieke

Beyens, Matthias

Fransen, Erik

Nasir, Abdul

Vandeweyer, Geert

Schepers, Anne

Rahmoun, Malika

van Beusekom, Ellen

Huentelman, Matt J.

Offeciers, Erwin

Dhooghe, Ingeborg

Huber, Alex

Van de Heyning, Paul

Zanetti, Diego

De Leenheer, Els M.R.

Gilissen, Christian

Hoischen, Alexander

Cremers, Cor W.

Verbist, Berit

de Brouwer, Arjan P.M.

Padberg, George W.

Pennings, Ronald

Kayserili, Hülya

Kremer, Hannie

Van Camp, Guy

van Bokhoven, Hans
License Information

Text and Data Mining valid from 2019-05-01

Text and Data Mining valid from 2019-05-01

Version of Record valid from 2022-01-19
More Information

This article is maintained by: Elsevier

Article Title: Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0300-5

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics