Correction: Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in FAM83G
更正:病例报告:由FAM83G基因致病性移码缺失引起的常染色体隐性掌跖角化症伴双侧听力丧失
期刊:Frontiers in Medicine
影响因子:3
doi:10.3389/fmed.2026.1779531
Mora-Gómez, Mónica; Feito, Marta; Gallego-Zazo, Natalia; Maseda-Pedrero, Rocío; Sobral-Costas, Tristán G; Miranda-Alcaraz, Lucía; Vásquez-Amell, Valeria; Rodríguez-Canó, Manuel; Parra, Alejandro; Cazalla, Mario; Arias, Pedro; Silván, Cristina; Jiménez-Estrada, Juan A; Ruiz-Pérez, Víctor L; Nevado, Julián; Lapunzina, Pablo; Tenorio-Castano, Jair