Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss. (2023)
Attributed to:
GEroscience and Multi-Morbidity: identifying targets for intervention (GEMM)
funded by
SPF
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1101/2023.04.27.23289040
PubMed Identifier: 37163093
Publication URI: http://europepmc.org/abstract/MED/37163093
Type: Journal Article/Review
Parent Publication: medRxiv : the preprint server for health sciences