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Literature DB >> 33750428

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.

Emanuele G Coci¹, Udo Koehler², Thomas Liehr³, Armin Stelzner⁴, Christian Fink⁵, Hendrik Langen⁴, Joachim Riedel⁴.

Abstract

Entities: Chemical Gene

Year: 2021 PMID： 33750428 PMCID： PMC7941681 DOI： 10.1186/s13039-021-00534-5

Source DB: PubMed Journal: Mol Cytogenet ISSN： 1755-8166 Impact factor: 2.009

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

Authors: Emanuele G Coci; Udo Koehler; Thomas Liehr; Armin Stelzner; Christian Fink; Hendrik Langen; Joachim Riedel
Journal: Mol Cytogenet Date: 2016-02-03 Impact factor: 2.009

1 in total