(Q31992388)

5 July 2017

A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patients (English)

1 reference

5 July 2017

6

1 reference

5 July 2017

Corona P

1

1 reference

5 July 2017

Antozzi C

2

1 reference

5 July 2017

Carrara F

3

1 reference

5 July 2017

D'Incerti L

4

1 reference

5 July 2017

Lamantea E

5

1 reference

5 July 2017

Zeviani M

7

1 reference

5 July 2017

language of work or name

1 reference

1 January 2001

1 reference

5 July 2017

5

1 reference

based on heuristic

inferred from page(s)

published in

Annals of Neurology

1 reference

5 July 2017

49

1 reference

5 July 2017

1

1 reference

5 July 2017

106-110

1 reference

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

5 July 2017

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28200101%2949%3A1%3C106%3A%3AAID-ANA16%3E3.0.CO%3B2-T

MELAS: clinical features, biochemistry, and molecular genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28200101%2949%3A1%3C106%3A%3AAID-ANA16%3E3.0.CO%3B2-T

The molecular basis and clinical characteristics of Maternally Inherited Diabetes and Deafness (MIDD), a recently recognized diabetic subtype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28200101%2949%3A1%3C106%3A%3AAID-ANA16%3E3.0.CO%3B2-T

Sequence and organization of the human mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28200101%2949%3A1%3C106%3A%3AAID-ANA16%3E3.0.CO%3B2-T

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28200101%2949%3A1%3C106%3A%3AAID-ANA16%3E3.0.CO%3B2-T

Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28200101%2949%3A1%3C106%3A%3AAID-ANA16%3E3.0.CO%3B2-T

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28200101%2949%3A1%3C106%3A%3AAID-ANA16%3E3.0.CO%3B2-T

10.1002/1531-8249(200101)49:1<106::AID-ANA16>3.0.CO;2-T

21 January 2018

Identifiers

DOI

1 reference

5 July 2017

1 reference