(Q50456010)
Statements
Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families. (English)
1 reference
Hashemzadeh Chaleshtori M
1 reference
Farrokhi E
1 reference
Dolati M
1 reference
Hoghooghi Rad L
1 reference
Amani Geshnigani S
1 reference
Crosby AH
1 reference
1 September 2007
1 reference
72
1 reference
3
1 reference
261-263
1 reference