(Q52201953)

English

The expanding clinical phenotype of the tRNA(Leu(UUR)) A-->G mutation at np 3243 of mitochondrial DNA: diabetic embryopathy associated with mitochondrial cytopathy.

scientific article published in April 1996

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scholarly article

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

The expanding clinical phenotype of the tRNA(Leu(UUR)) A-->G mutation at np 3243 of mitochondrial DNA: diabetic embryopathy associated with mitochondrial cytopathy. (English)

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

mitochondrial DNA

0 references

diabetic embryopathy

1 reference

based on heuristic

inferred from title

author name string

Feigenbaum A

1

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

Chitayat D

2

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

Robinson B

3

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

MacGregor D

4

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

Myint T

5

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

Arbus G

6

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

Nowaczyk MJ

7

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

publication date

1 April 1996

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

62

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

4

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

404-409

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

Type I diabetes mellitus and pregnancy

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

Hyperglycemia-induced teratogenesis is mediated by a functional deficiency of arachidonic acid

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observations.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

Brain damage due to asphyxia: mechanism of causation.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

Can prepregnancy care of diabetic women reduce the risk of abnormal babies?

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

Determinants of IDDM and Perinatal Mortality in Children of Diabetic Mothers

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819960424%2962%3A4%3C404%3A%3AAID-AJMG14%3E3.0.CO%3B2-S

21 January 2018

Identifiers

10.1002/(SICI)1096-8628(19960424)62:4<404::AID-AJMG14>3.0.CO;2-S

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

1 reference

Europe PubMed Central

26 April 2018

http://europepmc.org/abstract/MED/8723072

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