(Q28302643)

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Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis

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Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis (English)

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1 reference

L J Russell

1

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J J DiGiovanna

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2

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G R Rogers

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3

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P M Steinert

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4

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N Hashem

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5

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J G Compton

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6

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S J Bale

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7

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language of work or name

English

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publication date

March 1995

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published in

Nature Genetics

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volume

9

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issue

3

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page(s)

279-83

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cites work

Assignment of the human transglutaminase 2 (TGM2) and transglutaminase 3 (TGM3) genes to chromosome 20q11.2

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https://api.crossref.org/works/10.1038/NG0395-279

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21 April 2017

The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes.

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reference URL

https://api.crossref.org/works/10.1038%2FNG0395-279

retrieved

21 January 2018

The human tissue transglutaminase gene maps on chromosome 20q12 by in situ fluorescence hybridization

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https://api.crossref.org/works/10.1038%2FNG0395-279

retrieved

21 January 2018

Three-dimensional structure of a transglutaminase: human blood coagulation factor XIII

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https://api.crossref.org/works/10.1038%2FNG0395-279

retrieved

7 January 2021

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Transglutaminase factor XIII uses proteinase-like catalytic triad to crosslink macromolecules

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https://api.crossref.org/works/10.1038%2FNG0395-279

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7 January 2021

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Factor XIII ABristol 1: detection of a nonsense mutation (Arg171-->stop codon) in factor XIII A subunit deficiency

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https://api.crossref.org/works/10.1038%2FNG0395-279

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7 January 2021

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Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs

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reference URL

https://api.crossref.org/works/10.1038%2FNG0395-279

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7 January 2021

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Identifiers

DOI

10.1038/NG0395-279

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PubMed publication ID

7773290

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ResearchGate publication ID

15426485

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(Q28302643)

Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis

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