PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery
Paria Najarzadeh Torbati, Lukas Hallbrucker, Michaela A. H. Hofrichter…·Barbara Vona
The paper identifies a homozygous splice-site variant in PALM3 and a missense variant in OTOA in a family with autosomal recessive hearing loss, supporting PALM3 as a candidate gene through functional and comparative analysis.