(Q24539147)

2

0 references

F Saberi

3

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E Campeau

4

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H Y Hwang

5

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B Shane

6

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J A Phillips

7

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D S Rosenblatt

8

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R A Gravel

American Journal of Human Genetics

9

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language of work or name

English

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publication date

August 1998

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published in

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volume

63

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issue

2

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page(s)

409-14

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cites work

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377317

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

24 March 2017

1 reference

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Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

24 March 2017

1 reference

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Structure-based perspectives on B12-dependent enzymes

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377317

Human methionine synthase. cDNA cloning, gene localization, and expression

24 March 2017

1 reference

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Defects in human methionine synthase in cblG patients

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377317

Cloning, mapping and RNA analysis of the human methionine synthase gene

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377317

Defects in auxiliary redox proteins lead to functional methionine synthase deficiency

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377317

Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377317

The Yin-Yang of cobalamin biochemistry

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377317

Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377317

Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood

30 May 2018

1 reference

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Heterogeneity in cblG: Differential retention of cobalamin on methionine synthase

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377317

30 May 2018

Identifiers

DOI

10.1086/301976

1 reference

1 reference

1 reference

PubMed publication ID

9683607

1 reference