(Q71651329)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7523605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

title

Expression of P0 protein in sural nerve of a patient with hereditary motor and sensory neuropathy type III (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7523605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

Expression of Po protein in sural nerve of a patient with hereditary motor and sensory neuropathy type III (English)

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

hereditary motor and sensory neuropathy

16 May 2024

main subject

0 references

6

K. Hayasaka

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7523605

16 May 2024

author name string

N. Tachi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7523605

16 May 2024

K. Kasai

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7523605

16 May 2024

S. Chiba

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7523605

16 May 2024

M. Naganuma

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7523605

16 May 2024

K. Uyemura

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7523605

16 May 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7523605

16 May 2024

publication date

1 June 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7523605%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

20 October 2019

number of pages

4

1 reference

based on heuristic

inferred from page(s)

https://api.elsevier.com/content/article/PII:0022510X94900124?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

https://api.elsevier.com/content/article/PII:0022510X94900124?httpAccept=text/plain

16 May 2024

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

Journal of the Neurological Sciences

16 May 2024

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7523605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

volume

124

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7523605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7523605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

page(s)

67-70

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7523605%20AND%20SRC:MED&resulttype=core&format=json

Congenital absence of peripheral myelin: abnormal Schwann cell development causes lethal arthrogryposis multiplex congenita

20 October 2019

cites work

1

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

Hereditary demyelinating motor and sensory neuropathy

16 May 2024

3

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.

16 May 2024

4

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

Congenital hypomyelination polyneuropathy. Pathological findings compared with polyneuropathies starting later in life.

16 May 2024

5

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin

16 May 2024

6

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

16 May 2024

7

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin

16 May 2024

8

1 reference

https://api.crossref.org/works/10.1016/0022-510X(94)90012-4

16 May 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7523605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference