Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7. (Q35196453)

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22 September 2019

title

Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7 (English)

1 reference

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22 September 2019

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J Vilkki

1

1 reference

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22 September 2019

J Ott

2

1 reference

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22 September 2019

M L Savontaus

3

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22 September 2019

P Aula

4

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22 September 2019

E K Nikoskelainen

5

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22 September 2019

language of work or name

English

0 references

publication date

1 March 1991

1 reference

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American Journal of Human Genetics

22 September 2019

published in

1 reference

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22 September 2019

volume

48

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22 September 2019

issue

3

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22 September 2019

page(s)

486-491

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LEBER'S DISEASE IN THE NETHERLANDS.

22 September 2019

cites work

1 reference

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Strategies for multilocus linkage analysis in humans

13 July 2018

1 reference

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Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2.

13 July 2018

1 reference

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

13 July 2018

1 reference

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Report of the committee on linkage and gene order

13 July 2018

1 reference

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Norrie disease gene is distinct from the monoamine oxidase genes.

13 July 2018

1 reference

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Human monoamine oxidase A and B genes map to Xp 11.23 and are deleted in a patient with Norrie disease

13 July 2018

1 reference

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Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis

13 July 2018

1 reference

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Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

13 July 2018

1 reference

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Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

13 July 2018

1 reference

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Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.

13 July 2018

1 reference

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Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci

13 July 2018

1 reference

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Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis

13 July 2018

1 reference

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The inheritance of Leber's disease. A genealogical follow-up study

13 July 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/1998335

12 December 2020

The clinical findings in Leber's hereditary optic neuroretinopathy. Leber's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/1998335

12 December 2020

Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/1998335

12 December 2020

Human mitochondrial DNA types in Finland

1 reference

https://pubmed.ncbi.nlm.nih.gov/1998335

12 December 2020

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp

1 reference

https://pubmed.ncbi.nlm.nih.gov/1998335

12 December 2020

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1998335

12 December 2020

Norrie disease: Linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe

1 reference

https://pubmed.ncbi.nlm.nih.gov/1998335

12 December 2020

Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/1998335

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1998335%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

PubMed publication ID

1998335

1 reference