Crossmark

A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay

Crossref DOI link: https://doi.org/10.1038/s41436-018-0290-3

Published Print: 2019-05

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

Authors

Mucha, Bettina E.

Banka, Siddharth

Ajeawung, Norbert Fonya

Molidperee, Sirinart

Chen, Gary G.

Koenig, Mary Kay

Adejumo, Rhamat B.

Till, Marianne

Harbord, Michael

Perrier, Renee

Lemyre, Emmanuelle

Boucher, Renee-Myriam

Skotko, Brian G.

Waxler, Jessica L.

Thomas, Mary Ann

Hodge, Jennelle C.

Gecz, Jozef

Nicholl, Jillian

McGregor, Lesley

Linden, Tobias

Sisodiya, Sanjay M.

Sanlaville, Damien

Cheung, Sau W.

Ernst, Carl

Campeau, Philippe M.
License Information

Text and Data Mining valid from 2019-05-01

Version of Record valid from 2022-01-19

Text and Data Mining valid from 2019-05-01
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Article History

Received: 5 June 2018

Accepted: 17 August 2018

First Online: 24 September 2018

Change Date: 14 January 2019

Change Type: Correction

Change Details: The original version of this Article contained an error in the spelling of the author Siddharth Banka, which was incorrectly given as Siddhart Banka. This has now been corrected in both the PDF and HTML versions of the Article.

Disclosure

: The authors declare no conflicts of interest.