(Q30980046)

27 June 2017

title

Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia (English)

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27 June 2017

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3

Herawati Sudoyo

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author name string

Safarina G Malik

1

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27 June 2017

Nova Pieter

2

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27 June 2017

Herawati Sudoyo

3

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27 June 2017

Abdul Kadir

4

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27 June 2017

Sangkot Marzuki

5

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27 June 2017

publication date

3 September 2003

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Journal of Human Genetics

27 June 2017

published in

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27 June 2017

volume

48

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27 June 2017

issue

9

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27 June 2017

page(s)

480-483

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https://scigraph.springernature.com/pub.10.1007/s10038-003-0056-9

27 June 2017

exact match

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cites work

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A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

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A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I

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12 December 2020

Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.

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12 December 2020

Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene

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12 December 2020

The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan

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12 December 2020

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

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12 December 2020

Hearing loss due to the mitochondrial A1555G mutation in Italian families.

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12 December 2020

Mitochondrial genome and susceptibility to diabetes mellitus

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12 December 2020

The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.

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12 December 2020

Phenylketonuria (PKU): screening and management

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12 December 2020

Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey.

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12 December 2020

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

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12 December 2020

Prevalence of mitochondrial gene mutations among hearing impaired patients

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12 December 2020

Nonsyndromic sensorineural deafness associated with the A1555G mutation in the mitochondrial small subunit ribosomal RNA in a Balinese family

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12 December 2020

Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity.

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12 December 2020

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

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12 December 2020

Mitochondrial DNA A3243G mutation in patients with early- or late-onset type 2 diabetes mellitus in Hong Kong Chinese

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12 December 2020

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity

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12 December 2020

Challenge of epidemiological research in the developing world: overview.

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12 December 2020

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

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12 December 2020

Mitochondrial deafness mutations reviewed

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12 December 2020

10.1007/S10038-003-0056-9

Identifiers

DOI

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27 June 2017

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