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CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes

Crossref DOI link: https://doi.org/10.1186/s13039-016-0219-y

Published Online: 2016-02-03

Published Print: 2016-12

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

Authors

Coci, Emanuele G.

Koehler, Udo

Liehr, Thomas

Stelzner, Armin

Fink, Christian

Langen, Hendrik

Riedel, Joachim
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Text and Data Mining valid from 2016-02-03

Version of Record valid from 2016-02-03
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Article History

Received: 5 November 2015

Accepted: 26 January 2016

First Online: 3 February 2016

Change Date: 9 March 2021

Change Type: Correction

Change Details: A Correction to this paper has been published:

Change Details: https://doi.org/10.1186/s13039-021-00534-5

Updates are available Correction dated 2021-03-09

Click to view Correction: https://doi.org/10.1186/s13039-021-00534-5