Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment.

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Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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Frequency of mitochondrial m.1 ...... -syndromic hearing impairment.

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Frequency of mitochondrial m.1 ...... -syndromic hearing impairment.

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Frequency of mitochondrial m.1 ...... -syndromic hearing impairment.

@en

Frequency of mitochondrial m.1 ...... -syndromic hearing impairment.

@nl

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Frequency of mitochondrial m.1 ...... -syndromic hearing impairment.

@en

Frequency of mitochondrial m.1 ...... -syndromic hearing impairment.

@nl

P1476

Frequency of mitochondrial m.1 ...... -syndromic hearing impairment.

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Aftab Ali Shah

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Andreas Breß

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Hazem Kaheel

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Marlies Kniper

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Mohamed A Hassan

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Mutaz Amin

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Yousuf H Y Bakhit

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P2860

Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound

Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.

Screening for the mitochondrial A1555G mutation among Egyptian patients with non-syndromic, sensorineural hearing loss.

The genetic bases for non-syndromic hearing loss among Chinese

Prevalence of consanguineous marriages in Syria.

Audiological and genetic features of the mtDNA mutations.

Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.

GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population.

Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.

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s12901-018-0055-2

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scholarly article

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10.1186/S12901-018-0055-2

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P577

2018-05-21T00:00:00Z

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1104137508

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29942192

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5963064

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