(Q41667283)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

Maternally inherited nonsyndromic hearing loss (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

author name string

R A Friedman

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Y Bykhovskaya

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

C M Sue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

S DiMauro

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

R Bradley

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

R Fallis-Cunningham

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

N Paradies

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

M L Pensak

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

J Groden

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

X C Li

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

N Fischel-Ghodsian

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

publication date

1 June 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part A

8 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

volume

84

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

page(s)

369-372

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

Audiovestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides.

8 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12s rRNA gene: evidence of heteroplasmy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

Mitochondrial mutation associated with nonsyndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990604%2984%3A4%3C369%3A%3AAID-AJMG12%3E3.0.CO%3B2-V

10.1002/(SICI)1096-8628(19990604)84:4<369::AID-AJMG12>3.0.CO;2-V

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10340654%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference