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A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis

Crossref DOI link: https://doi.org/10.1186/s40478-018-0610-5

Published Online: 2018-10-19

Published Print: 2018-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Vezain, Myriam

Lecuyer, Matthieu

Rubio, Marina

Dupé, Valérie

Ratié, Leslie

David, Véronique

Pasquier, Laurent

Odent, Sylvie

Coutant, Sophie

Tournier, Isabelle

Trestard, Laetitia

Adle-Biassette, Homa

Vivien, Denis

Frébourg, Thierry

Gonzalez, Bruno J

Laquerrière, Annie

Saugier-Veber, Pascale https://orcid.org/0000-0001-5601-3415
Funding

Funding for this research was provided by:

European Regional Development Fund
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Article History

Received: 27 September 2018

Accepted: 29 September 2018

First Online: 19 October 2018

Ethics approval

: All procedures were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

: The authors declare that they have no competing interest.

: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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