(Q71395997)

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A missense mutation in the neurofibromatosis 2 gene occurs in patients with mild and severe phenotypes

scientific article published on 01 August 1996

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scholarly article

1 reference

stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

title

A missense mutation in the neurofibromatosis 2 gene occurs in patients with mild and severe phenotypes (English)

1 reference

stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

main subject

neurofibromatosis type II

1 reference

D R Scoles

1

1 reference

stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

M E Baser

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

S M Pulst

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

language of work or name

English

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publication date

1 August 1996

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stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

volume

47

1 reference

stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

issue

2

1 reference

stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

page(s)

544-546

1 reference

stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

retrieved

18 October 2019

Identifiers

DOI

10.1212/WNL.47.2.544

1 reference

stated in

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference

Europe PubMed Central

PubMed ID

8757035

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8757035%20AND%20SRC:MED&resulttype=core&format=json

(Q71395997)

A missense mutation in the neurofibromatosis 2 gene occurs in patients with mild and severe phenotypes

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