&lt;i&gt;GJB2&lt;/i&gt;Gene Related Nonsyndromic Hearing Loss in Mazandaran Province

GJB2Gene Related Nonsyndromic Hearing Loss in Mazandaran Province

来源 :遗传学期刊(英文) | 被引量 : 0次 | 上传用户：mimibbs

【摘要】

：

Introduction: Congenital hearing loss is the most common sensory deficit in the world and mutations in GJB2 gene are the most common c

【作者】

：

Elaheh Hosseini Seyed Saeid Mo

【机构】

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NovinGeneticDiagnosticLaboratory,MehreganGeneticCounselingCenter,NovinGeneticCounselingCenter,Geneti

【出处】

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遗传学期刊(英文)

【发表日期】

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2020年3期

【关键词】

：

Hearing Loss GJB2 Mazandaran Hereditary Deafness NONSYNDROMIC Hearing Loss GJB2

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Introduction: Congenital hearing loss is the most common sensory deficit in the world and mutations in GJB2 gene are the most common cause of deafness in many populations. Frequency of GJB2</e

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