A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy - Concepedia

Concepedia

Publication | Open Access

A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy

DOI Full Paper Access

44

Citations

43

References

2018

Year

Svein I. Støve, Marina Blenski, Asbjørg Stray‐Pedersen, Klaas J. Wierenga, Shalini N. Jhangiani, Zeynep Coban‐Akdemir, David L. Crawford, Nina McTiernan, Line M. Myklebust, Gabriela Purcarin,

European Journal of Human Genetics

CardiomyopathyDevelopmental BiologyMolecular PhysiologyTranslational BiologyGenetic DisorderGeneticsMolecular GeneticsHypertrophic CardiomyopathyDisease Gene IdentificationMedicineNovel Naa10 Variant

References

	Year	Citations

Page 1

Page 1