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

Detalles Bibliográficos
Autores principales: Coci, Emanuele G., Koehler, Udo, Liehr, Thomas, Stelzner, Armin, Fink, Christian, Langen, Hendrik, Riedel, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941681/
https://www.ncbi.nlm.nih.gov/pubmed/33750428
http://dx.doi.org/10.1186/s13039-021-00534-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941681/
https://www.ncbi.nlm.nih.gov/pubmed/33750428
http://dx.doi.org/10.1186/s13039-021-00534-5

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