(Q35131653)

6 August 2017

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title

A major step on the road to understanding a unique posttranslational modification and its role in a genetic disease (English)

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6 August 2017

Jacques U Baenziger

1

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6 August 2017

language of work or name

English

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publication date

1 May 2003

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6 August 2017

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6 August 2017

volume

113

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6 August 2017

issue

4

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6 August 2017

page(s)

421-422

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Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency.

6 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900354-4

7 January 2021

The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900354-4

7 January 2021

Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900354-4

7 January 2021

The sulfatase gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900354-4

7 January 2021

A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2803%2900354-4

7 January 2021

10.1016/S0092-8674(03)00354-4

Identifiers

DOI

1 reference

6 August 2017

1 reference