(Q24540317)

1

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M Zeviani

2

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G P Comi

3

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M G Piscaglia

4

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L Peltonen

5

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A Suomalainen

American Journal of Human Genetics

6

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language of work or name

English

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publication date

July 1999

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published in

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volume

65

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page(s)

256-61

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issue

1

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cites work

Muscle-nerve involvement in autosomal dominant progressive external ophthalmoplegia with hypogonadism

1 reference

7 January 2021

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

1 reference

7 January 2021

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

1 reference

7 January 2021

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1 reference

7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

7 January 2021

An autosomal locus predisposing to deletions of mitochondrial DNA

1 reference

7 January 2021

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

1 reference

7 January 2021

Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4

1 reference

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

7 January 2021

Computer-simulation methods in human linkage analysis

1 reference

7 January 2021

Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter.

1 reference

7 January 2021

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

1 reference

7 January 2021

Assignment of the human muscle adenine nucleotide translocator gene (ANT1) to 4q35 by fluorescence in situ hybridization

1 reference

7 January 2021

Avoiding recomputation in linkage analysis.

1 reference

7 January 2021

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

1 reference

7 January 2021

A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome

1 reference

7 January 2021

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies

1 reference

7 January 2021

Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.

1 reference

7 January 2021