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

Affiliations

Emanuele G. Coci: Center of Social Pediatrics and Pediatric Neurology, General Hospital of Celle
Udo Koehler: Medizinisch Genetisches Zentrum
Thomas Liehr: Institute of Human Genetics, Friedrich Schiller University, Jena University Hospital
Armin Stelzner: Center of Social Pediatrics and Pediatric Neurology, General Hospital of Celle
Christian Fink: Department of Radiology, General Hospital of Celle
Hendrik Langen: Center of Social Pediatrics and Pediatric Neurology, General Hospital of Celle
Joachim Riedel: Center of Social Pediatrics and Pediatric Neurology, General Hospital of Celle

Abstract

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