(Q71457520)

English

[A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation]

scientific article published on 01 July 1995

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Europe PubMed Central

PubMed publication ID

8777804

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

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18 October 2019

title

[A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation] (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8777804

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

main subject

hereditary motor and sensory neuropathy

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author name string

Ohnishi A

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1

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Europe PubMed Central

PubMed publication ID

8777804

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

Yoshimura T

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2

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PubMed publication ID

8777804

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

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18 October 2019

Kanehisa Y

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3

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PubMed publication ID

8777804

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

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18 October 2019

Fukushima Y

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4

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PubMed publication ID

8777804

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

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18 October 2019

publication date

1 July 1995

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Europe PubMed Central

PubMed publication ID

8777804

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference

Europe PubMed Central

PubMed publication ID

8777804

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

volume

35

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PubMed publication ID

8777804

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

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18 October 2019

issue

7

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PubMed publication ID

8777804

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18 October 2019

page(s)

788-792

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PubMed publication ID

8777804

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

Identifiers

PubMed publication ID

8777804

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8777804

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8777804%20AND%20SRC:MED&resulttype=core&format=json

(Q71457520)

[A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation]

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