Leticia Labat-de-Hoz

No ORCID on file · 1 paper in corpus
review 2021
Cells ·doi:10.3390/cells10102554

Almost 25 years have passed since a mutation of a formin gene, DIAPH1, was identified as being responsible for a human inherited disorder: a form of sensorineural hearing loss. Since then, our knowledge of the links between formins and dise…