(Q52862227)

English

A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees.

scientific article published in November 2001

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Europe PubMed Central

PubMed publication ID

11726555

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9 May 2018

reference URL

http://europepmc.org/abstract/MED/11726555

title

A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees. (English)

1 reference

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Europe PubMed Central

PubMed publication ID

11726555

retrieved

9 May 2018

reference URL

http://europepmc.org/abstract/MED/11726555

author name string

Harland M

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1

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Europe PubMed Central

PubMed publication ID

11726555

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9 May 2018

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http://europepmc.org/abstract/MED/11726555

Mistry S

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2

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Europe PubMed Central

PubMed publication ID

11726555

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9 May 2018

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http://europepmc.org/abstract/MED/11726555

Bishop DT

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3

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PubMed publication ID

11726555

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9 May 2018

reference URL

http://europepmc.org/abstract/MED/11726555

Bishop JA

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4

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PubMed publication ID

11726555

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9 May 2018

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http://europepmc.org/abstract/MED/11726555

publication date

1 November 2001

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11726555

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9 May 2018

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http://europepmc.org/abstract/MED/11726555

published in

Human Molecular Genetics

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PubMed publication ID

11726555

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9 May 2018

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http://europepmc.org/abstract/MED/11726555

volume

10

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issue

23

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2679-2686

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11726555

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9 May 2018

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DOI

10.1093/HMG/10.23.2679

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11726555

retrieved

9 May 2018

reference URL

http://europepmc.org/abstract/MED/11726555

PubMed publication ID

11726555

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11726555

retrieved

9 May 2018

reference URL

http://europepmc.org/abstract/MED/11726555

ResearchGate publication ID

276944322

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(Q52862227)

A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees.

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