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Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

Crossref DOI link: https://doi.org/10.1186/s13229-019-0271-7

Published Online: 2019-05-03

Published Print: 2019-12

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

Authors

Baker, Emma K. https://orcid.org/0000-0003-1165-0490
Arpone, Marta

Aliaga, Solange M.

Bretherton, Lesley

Kraan, Claudine M.

Bui, Minh

Slater, Howard R.

Ling, Ling

Francis, David

Hunter, Matthew F.

Elliott, Justine

Rogers, Carolyn

Field, Michael

Cohen, Jonathan

Cornish, Kim

Santa Maria, Lorena

Faundes, Victor

Curotto, Bianca

Morales, Paulina

Trigo, Cesar

Salas, Isabel

Alliende, Angelica M.

Amor, David J.

Godler, David E.
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Article History

Received: 30 January 2019

Accepted: 3 April 2019

First Online: 3 May 2019

Ethics approval and consent to participate

: All procedures were approved by The Royal Children’s Hospital and INTA Human Research Ethics Committees (HREC #33066 and #15, respectively). All parents/caregivers provided written informed consent and those who were deemed cognitively able also provided written informed consent.

: D. Godler is an inventor of the following patents: PCT/AU2010/001134; filing No. AU2010/903595; filing No. AU2011/902500; and filing No. 2013/900227, related to the technology described in this publication. All other authors have no conflicts of interest to declare.

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