(Q81614837)
Statements
Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in the SLC26A4 gene in siblings (English)
Arellano B
Ramírez-Camacho R
Villamar M
Trinidad A
García JR
Moreno F
Hernández-Chico C