First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.
Al-Achkar, Walid
First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss. [electronic resource] - International journal of pediatric otorhinolaryngology Jan 2017 - 82-87 p. digital
Publication Type: Journal Article
1872-8464
10.1016/j.ijporl.2016.11.015 doi
Connexin 26
Connexin 30
Connexins--genetics
Exons
Female
Genotype
Hearing Loss, Sensorineural--genetics
Heterozygote
Humans
Male
Multiplex Polymerase Chain Reaction
Mutation
Polymerase Chain Reaction
Polymorphism, Restriction Fragment Length
Sequence Deletion
Syria
First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss. [electronic resource] - International journal of pediatric otorhinolaryngology Jan 2017 - 82-87 p. digital
Publication Type: Journal Article
1872-8464
10.1016/j.ijporl.2016.11.015 doi
Connexin 26
Connexin 30
Connexins--genetics
Exons
Female
Genotype
Hearing Loss, Sensorineural--genetics
Heterozygote
Humans
Male
Multiplex Polymerase Chain Reaction
Mutation
Polymerase Chain Reaction
Polymorphism, Restriction Fragment Length
Sequence Deletion
Syria