Canuto EM

No ORCID on file · 1 paper in corpus
2022
Frontiers in genetics ·doi:10.3389/fgene.2022.995947

Background: Alström syndrome (AS) is an ultrarare multisystemic progressive disease caused by autosomal recessive variations of the ALMS1 gene (2p13). AS is characterized by double sensory impairment, cardiomyopathy, childhood obesity, extr…