A rare haplotype of the GJD3 gene segregating in familial Meniere's disease interferes with connexin assembly.
Escalera-Balsera A, Robles-Bolivar P, Parra-Perez AM, Murillo-Cuesta S, Chua HC, Rodríguez-de la Rosa L, Contreras J, Domarecka E, Amor-Dorado JC, Soto-Varela A, Varela-Nieto I, Szczepek AJ, Gallego-Martinez A, Lopez-Escamez JA.
Escalera-Balsera A, et al. Among authors: contreras j.
Genome Med. 2025 Jan 15;17(1):4. doi: 10.1186/s13073-024-01425-1.
Genome Med. 2025.
PMID: 39815343
Free PMC article.