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Autosomal Recessive 21 Deafness
mutation in TECTA
Also Known As:
Deafness, Autosomal Recessive 21; DFNB21
Networked:
1
relevant articles (
0
outcomes,
0
trials/studies)
Disease Context: Research Results
Otorhinolaryngologic Diseases: 203
Ear Diseases: 261
Hearing Disorders: 325
Hearing Loss: 12265
Sensorineural Hearing Loss: 3974
Autosomal Recessive 21 Deafness: 1
Nervous System Diseases: 14178
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Sensorineural Hearing Loss: 3974
Autosomal Recessive 21 Deafness: 1
Signs and Symptoms Pathological Conditions
Signs and Symptoms
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Sensorineural Hearing Loss: 3974
Autosomal Recessive 21 Deafness: 1
Experts
1.
Ahangari, Najmeh
: 1 article (05/2016)
2.
Masoudi, Marjan
: 1 article (05/2016)
3.
Nejatizadeh, Azim
: 1 article (05/2016)
4.
Poursadegh Zonouzi, Ahmad
: 1 article (05/2016)
5.
Poursadegh Zonouzi, Ali Akbar
: 1 article (05/2016)
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Autosomal Recessive 21 Deafness:
1.
polyacrylamide
IBA
05/01/2016 - "
Negative samples for GJB2 gene mutations were analyzed for the linkage to DFNB3, DFNB9 and DFNB21 loci by genotyping the corresponding short tandem repeat (STR) markers using polymerase chain reaction (PCR) and polyacrylamide gel electrophoresis (PAGE) methods.
"