Gene: [07q3/DFNB13] deafness, autosomal recessive 13;
|
REF |
PAT,LOC,LIN "Mustapha M &: Eur J Hum Genet, 6, 245-250, 1998 |
|
KEY |
neu |
|
CLA |
unknown, basic |
|
LOC |
07 q34-36 |
|
MIM |
MIM: 603098 |
Ссылки:
- Gene: [13q11/GJB2] gap junction protein, beta 2, 26 kD (connexin 26); deafness, autosomal dominant 3 (DFNA3; MIM:601544); deafness, autosomal recessive 1 (DFNB1; MIM:220290); [CX26 NSRD1 ]
- Gene: [07q31/PDS] pendrin (86kD); Pendred syndrome (goitre and sensorineural hearing loss); thyroid hormonogenesis, genetic defect in, IIB; deafness, autosomal recessive 4 (MIM:600791); [DFNB4 ]
