(Q44295292)

1 December 2017

Prenatal diagnosis of succinate semialdehyde dehydrogenase deficiency in non-identical twins (English)

1 reference

1 December 2017

I A Aligianis

1

1 reference

1 December 2017

P A Farndon

2

1 reference

1 December 2017

R G F Gray

3

1 reference

1 December 2017

S K Heath

4

1 reference

1 December 2017

M Kilby

5

1 reference

1 December 2017

K M Gibson

6

1 reference

1 December 2017

S Akaboshi

7

1 reference

1 December 2017

1 October 2002

1 reference

Journal of Inherited Metabolic Disease

1 December 2017

1 reference

1 December 2017

25

1 reference

1 December 2017

6

1 reference

1 December 2017

517-518

1 reference

https://scigraph.springernature.com/pub.10.1023/a:1021215605013

1 December 2017

0 references

cites work

Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analyses.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12555945

PubMed

reference URL

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12555945

PubMed

reference URL

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1023/A:1021215605013

1 reference

Dimensions Publication ID

1 December 2017

0 references

1 reference