(Q34385881)

1 August 2017

The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3. (English)

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1 August 2017

Nicholson GA

1

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1 August 2017

Dawkins JL

2

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1 August 2017

Blair IP

3

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1 August 2017

Kennerson ML

4

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1 August 2017

Gordon MJ

5

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1 August 2017

Cherryson AK

6

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1 August 2017

Nash J

7

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1 August 2017

Bananis T

8

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1 August 2017

language of work or name

English

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publication date

1 May 1996

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1 August 2017

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1 August 2017

13

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1 August 2017

1

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1 August 2017

101-104

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https://scigraph.springernature.com/pub.10.1038/ng0596-101

1 August 2017

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cites work

The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

Cloning and chromosomal localization of the human TRK-B tyrosine kinase receptor gene (NTRK2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

Molecular genetics of neuronal survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

CEPH Consortium Map of Chromosome 9

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

Familial ulcers, mutilating lesions of the extremities, and acro-osteolysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Hereditary sensory radicular neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994.

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Structure, function, and chromosome mapping of the growth-suppressing human homologue of the murine gas1 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Transgenic and knock-out mice: models of neurological disease.

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Location cloning strategy for characterizing genetic defects in Huntington's disease and Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Positional cloning moves from perditional to traditional

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

The 1993-94 Généthon human genetic linkage map

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https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

https://api.crossref.org/works/10.1038%2FNG0596-101

7 January 2021

Identifiers

DOI

10.1038/NG0596-101

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Dimensions Publication ID

1 August 2017

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