(Q77732496)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

title

Detection of DNA mutations associated with mitochondrial diseases by Agilent 2100 bioanalyzer (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

author name string

Ching-You Lu

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

Dan-Ju Tso

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

Tom Yang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

Yuh-Jyh Jong

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

publication date

1 April 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

volume

318

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

issue

1-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

page(s)

97-105

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

Sequence and organization of the human mitochondrial genome

7 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

Mitochondrial DNA sequence variation in human evolution and disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

Mitochondrial DNA alterations and genetic diseases: a review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

Agilent 2100 bioanalyzer for restriction fragment length polymorphism analysis of the Campylobacter jejuni flagellin gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

Protein sizing on a microchip

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

Mitochondrial DNA mutation in a Chinese family with myoclonic epilepsy and ragged-red fiber disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

Myoclonic epilepsy with ragged-red fibers (MERRF) syndrome: report of a Chinese family with mitochondrial DNA point mutation in tRNA(Lys) gene.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900809-9

10.1016/S0009-8981(01)00809-9

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11880118%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference