[Study of deafness associated with DFNB59 gene [Pejvakin] mutation in Fars province]

S., Raeisi; E., Farokhi; M., Taherzadeh; F., Azadegan; M., Abolhasani; M., Raeisi; G., Banitalebi; A., Esmaili; R., Zaker; M., Hashemzadeh

S., Raeisi; E., Farokhi; M., Taherzadeh; F., Azadegan; M., Abolhasani; M., Raeisi; G., Banitalebi; A., Esmaili; R., Zaker; M., Hashemzadeh.

Qom University of Medical Sciences Journal. 2011; 4 (4): 10-15

in Fa | IMEMR | ID: emr-110575

Responsible library: EMRO

Subject(s)

Humans; Female; Male; Deafness/etiology; Nerve Tissue Proteins; Mutation/genetics; Hearing Loss

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Index: IMEMR Main subject: Deafness / Hearing Loss / Mutation / Nerve Tissue Proteins Limits: Female / Humans / Male Language: Fa Journal: Qom Univ. Med. Sci. J. Year: 2011

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Index: IMEMR Main subject: Deafness / Hearing Loss / Mutation / Nerve Tissue Proteins Limits: Female / Humans / Male Language: Fa Journal: Qom Univ. Med. Sci. J. Year: 2011