(Q34281921)

1 August 2017

CKN1 (MIM 216400): mutations in Cockayne syndrome type A and a new common polymorphism (English)

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1 August 2017

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4

Robert A Hegele

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author name string

Henian Cao

series ordinal

1

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PubMed ID

14661080

1 August 2017

Christina Williams

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2

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PubMed ID

14661080

1 August 2017

Monica Carter

series ordinal

3

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1 August 2017

6 December 2003

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Journal of Human Genetics

1 August 2017

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1 August 2017

49

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1 August 2017

1

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1 August 2017

61-63

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https://scigraph.springernature.com/pub.10.1007/s10038-003-0107-2

1 August 2017

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cites work

The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH

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12 December 2020

Cockayne syndrome: Review of 140 cases

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12 December 2020

A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy

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12 December 2020

Three novel mutations responsible for Cockayne syndrome group A.

1 reference

12 December 2020

Mechanisms of transcription-coupled DNA repair

1 reference

12 December 2020

10.1007/S10038-003-0107-2

Identifiers

DOI

1 reference

1 August 2017

1 reference

PubMed ID

14661080