(Q34476065)

2 August 2017

title

Meesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene (English)

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Meesmann corneal dystrophy

2 August 2017

main subject

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Olivia Nichini

1

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2 August 2017

Violaine d'Allèves Manzi

series ordinal

2

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2 August 2017

Francis L Munier

series ordinal

3

1 reference

2 August 2017

Daniel F Schorderet

series ordinal

4

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2 August 2017

publication date

1 December 2005

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2 August 2017

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2 August 2017

volume

26

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2 August 2017

issue

4

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2 August 2017

page(s)

169-173

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The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

Heterozygous Ala137Pro mutation in keratin 12 gene found in Japanese with Meesmann's corneal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann's corneal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

Human keratin diseases: hereditary fragility of specific epithelial tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810500374391

10.1080/13816810500374391

21 January 2018

Identifiers

DOI

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2 August 2017

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