(Q57577956)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

Novel mutation in the HSN2 gene in a Korean patient with hereditary sensory and autonomic neuropathy type 2 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

hereditary sensory and autonomic neuropathy type 2

29 December 2019

main subject

0 references

1 reference

1 reference

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

3

Yeon-Lim Suh

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

author name string

Hyun-Jung Cho

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Byoung Joon Kim

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Jae-Young An

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

publication date

1 September 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

29 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

page(s)

905-908

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10038-006-0033-1

29 December 2019

exact match

0 references

cites work

Hereditary sensory neuropathy, type II. Clinical, electrophysiologic, histologic, and biochemical studies of a Quebec kinship.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10038-006-0033-1

Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates

21 January 2018

1 reference

12 December 2020

Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type II

1 reference

12 December 2020

A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family

1 reference

12 December 2020

Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians

1 reference

12 December 2020

New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2.

1 reference

12 December 2020

Congenital sensory neuropathy

1 reference

12 December 2020

Genetic heterogeneity of hereditary sensory neuropathy

1 reference

12 December 2020

10.1007/S10038-006-0033-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16946995%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference