Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes-Reference-Cited by-同舟云学术

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

Published:2021-03-09 Issue:1 Volume:14 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Coci Emanuele G.,Koehler Udo,Liehr Thomas,Stelzner Armin,Fink Christian,Langen Hendrik,Riedel Joachim

Abstract

An amendment to this paper has been published and can be accessed via the original article.

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-021-00534-5.pdf

Reference1 articles.

1. Coci EC, et al. CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes. Mol Cytogenet. 2016;9:10. https://doi.org/10.1186/s13039-016-0219-y.

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