(Q46910655)

English

Methionine adenosyltransferase (MAT) I/III deficiency with concurrent hyperhomocysteinaemia: two novel cases

scientific article published in January 2005

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

Methionine adenosyltransferase (MAT) I/III deficiency with concurrent hyperhomocysteinaemia: two novel cases (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

author name string

M Linnebank

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

F Lagler

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

A C Muntau

3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

W Röschinger

4

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

B Olgemöller

5

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

B Fowler

6

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

H G Koch

7

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

28

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

6

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

1167-1168

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

https://scigraph.springernature.com/pub.10.1007/s10545-005-4497-5

0 references

Molecular genetics of hepatic methionine adenosyltransferase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435220

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435220

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16435220

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10545-005-4497-5

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16435220

ResearchGate publication ID

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