(Q33680222)
Statements
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2) (English)
N J Lench
A F Markham
R F Mueller
R J Smith
P J Willems
I Schatteman
H Capon
G Van Camp
1 February 1998