(Q43542179)

24 November 2017

title

The first case of 4-hydroxybutyric aciduria in Japan (English)

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24 November 2017

5

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24 November 2017

Ishiguro Y

1

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24 November 2017

Kajita M

2

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24 November 2017

Aoshima T

3

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24 November 2017

Watanabe K

4

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24 November 2017

Yamaguchi S

6

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24 November 2017

publication date

1 March 2001

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24 November 2017

published in

Brain and Development

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24 November 2017

volume

23

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24 November 2017

issue

2

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24 November 2017

page(s)

128-130

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Inherited disorders of GABA metabolism

24 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900181-4

7 January 2021

4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900181-4

7 January 2021

The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900181-4

7 January 2021

Diagnosis and management of glutaric aciduria type I.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900181-4

7 January 2021

Human Succinic Semialdehyde Dehydrogenase

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900181-4

7 January 2021

Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900181-4

7 January 2021

Vigabatrin therapy in six patients with succinic semialdehyde dehydrogenase deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900181-4

7 January 2021

10.1016/S0387-7604(01)00181-4

Identifiers

DOI

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24 November 2017

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