Investigation of the A1555G mutation in mitochondrial DNA (MT-RNR1) in groups of Brazilian individuals with nonsyndromic deafness and normal-hearing.

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Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry.Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals.

P2860

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Investigation of the A1555G mutation in mitochondrial DNA (MT-RNR1) in groups of Brazilian individuals with nonsyndromic deafness and normal-hearing.

Item

http://www.wikidata.org/entity/Q43075490

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

@zh-hant

name

Investigation of the A1555G mu ...... c deafness and normal-hearing.

@en

Investigation of the A1555G mutation in mitochondrial DNA

@nl

type

Item

label

Investigation of the A1555G mu ...... c deafness and normal-hearing.

@en

Investigation of the A1555G mutation in mitochondrial DNA

@nl

prefLabel

Investigation of the A1555G mu ...... c deafness and normal-hearing.

@en

Investigation of the A1555G mutation in mitochondrial DNA

@nl

P1476

Investigation of the A1555G mu ...... c deafness and normal-hearing.

@en

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Christiane Maria Ayo

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

Karina Bezerra Salomão

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

Valter Augusto Della-Rosa

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

P2860

Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment

Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia.

Sensorineural hearing loss associated with the mitochondrial mutations.

Maternally inherited hearing impairment.

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

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.

Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk?

mtDNA mutations, hearing loss and aminoglycoside treatment in Mexicans.

Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.

P304

54-57

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P31

scholarly article

P356

10.4103/0971-6866.112888

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P433

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

P478

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

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2013-01-01T00:00:00Z

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P698

23901193

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P921

mitochondrial DNA

P932

3722630

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

Investigation of the A1555G mutation in mitochondrial DNA (MT-RNR1) in groups of Brazilian individuals with nonsyndromic deafness and normal-hearing.

about

P2860

P2860

Investigation of the A1555G mutation in mitochondrial DNA (MT-RNR1) in groups of Brazilian individuals with nonsyndromic deafness and normal-hearing.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932