"Severe intellectual disability with cardiac and dermatologic involvement due to homozygous METTL23 frameshift mutation: a case report of two Turkish sisters".


Besnek M., Aynekin B., Güleç A., Efthymiou S., Per H.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, cilt.47, sa.8, 2026 (SCI-Expanded, Scopus)