(Q42808822)

English

The M581V mutation, associated with a mild form of congenital insensitivity to pain with anhidrosis, causes partial inactivation of the NTRK1 receptor.

scientific article published on October 2002

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12406349%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

The M581V mutation, associated with a mild form of congenital insensitivity to pain with anhidrosis, causes partial inactivation of the NTRK1 receptor (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12406349%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

congenital disorder

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congenital insensitivity to pain with anhidrosis

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Marco A. Pierotti

3

1 reference

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14 December 2019

4

1 reference

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14 December 2019

2

object named as

Silvia Selleri

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14 December 2019

author name string

Claudia Miranda

1

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14 December 2019

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publication date

1 October 2002

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14 December 2019

Journal of Investigative Dermatology

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14 December 2019

119

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14 December 2019

4

1 reference

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14 December 2019

978-979

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14 December 2019

https://scigraph.springernature.com/pub.10.1046/j.1523-1747.2002.00140.x

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Identifiers

10.1046/J.1523-1747.2002.00140.X

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12406349%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

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1 reference

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14 December 2019

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