Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.

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Recent Advancements in the Regeneration of Auditory Hair Cells and Hearing Restoration Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.Acquired sensorineural hearing loss in children: current research and therapeutic perspectives.

P2860

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P2860

Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.

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Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.

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Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.

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P1476

Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.

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P2093

Duan Ma

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Fei Liu

http://www.w3.org/2001/XMLSchema#string

Wenjun Xia

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P2860

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene.

Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation

A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing loss

Distinctive audiometric profile associated with DFNB21 alleles of TECTA

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagen

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6

P2888

s11684-016-0449-8

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137-142

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scholarly article

review article

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10.1007/S11684-016-0449-8

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Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.

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P2860

P2860

Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.

description

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type

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prefLabel

P1433

P1476

P2093

P2860

P2888

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P31

P356

P433

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P577

P6179

P698

P356

P1433

P1476

P2093

P2860

P2888

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P433

P478

P577

P6179

P698