(Q28293123)

2

object named as

Raquel Dodelson de Kremer

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author name string

Celia J Angaroni

1

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Raquel Dodelson de Kremer

2

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Carlos E Argaraña

3

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Ana E Paschini-Capra

4

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Alicia N Giner-Ayala

5

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Roberto J Pezza

6

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Chi-Jiunn Pan

7

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Janice Y Chou

Molecular Genetics and Metabolism

8

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language of work or name

English

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publication date

November 2004

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published in

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volume

83

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issue

3

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page(s)

276-9

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cites work

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.06.010

Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.06.010

Transmembrane topology of glucose-6-phosphatase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.06.010

The molecular basis of glycogen storage disease type 1a: structure and function analysis of mutations in glucose-6-phosphatase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.06.010

An improved micromethod for the determination of glucose-6-phosphatase activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.06.010

A new microtechnique for the analysis of the human hepatic microsomal glucose-6-phosphatase system

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.06.010

Lactacystin, proteasome function, and cell fate

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.06.010

Molecular genetics of type 1 glycogen storage disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.06.010