(Q43981250)

28 November 2017

title

Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32. (English)

1 reference

28 November 2017

Zoran Brkanac

1

1 reference

28 November 2017

Magali Fernandez

2

1 reference

28 November 2017

Mark Matsushita

3

1 reference

28 November 2017

Hilary Lipe

4

1 reference

28 November 2017

John Wolff

5

1 reference

28 November 2017

Thomas D Bird

6

1 reference

28 November 2017

Wendy H Raskind

7

1 reference

28 November 2017

publication date

1 May 2002

1 reference

American Journal of Medical Genetics Part A

28 November 2017

published in

1 reference

28 November 2017

volume

114

1 reference

28 November 2017

issue

4

1 reference

28 November 2017

page(s)

450-457

1 reference

Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy and peripheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23.

28 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Comprehensive human genetic maps: individual and sex-specific variation in recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Familial cerebellar ataxia and hypogonadism associated with sensorimotor axonal polyneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Strategies for multilocus linkage analysis in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Friedreich's ataxia: clinical aspects and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Avoiding recomputation in linkage analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Phenotype-genotype correlations in a CMT2B family with refined 3q13-q22 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Peripheral neuropathy in spinocerebellar degenerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

Autosomal dominant cerebellar phenotypes: the genotype has settled the issue

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

A new variant of sensory ataxic neuropathy with autosomal dominant inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10361

21 January 2018

Identifiers

DOI

10.1002/AJMG.10361

1 reference

28 November 2017

1 reference