(Q45569163)

14 December 2017

title

S-adenosylhomocysteine hydrolase deficiency: two siblings with fetal hydrops and fatal outcomes (English)

1 reference

14 December 2017

S‐adenosylhomocysteine hydrolase deficiency: two siblings with fetal hydrops and fatal outcomes (English)

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9171-X

16 July 2024

1 reference

9

S Harvey Mudd

1 reference

14 December 2017

Randall Grubbs

1

1 reference

14 December 2017

Oliver Vugrek

2

1 reference

14 December 2017

Jeremy Deisch

3

1 reference

14 December 2017

Conrad Wagner

4

1 reference

14 December 2017

Sally Stabler

5

1 reference

14 December 2017

Robert Allen

6

1 reference

14 December 2017

Ivo Barić

7

1 reference

14 December 2017

Marko Rados

8

1 reference

14 December 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20852937

16 July 2024

publication date

18 September 2010

1 reference

full work available at URL

14 December 2017

https://onlinelibrary.wiley.com/doi/pdf/10.1007/s10545-010-9171-x

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9171-X

https://onlinelibrary.wiley.com/doi/full-xml/10.1007/s10545-010-9171-x

16 July 2024

1 reference

https://api.crossref.org/works/10.1007/S10545-010-9171-X

Journal of Inherited Metabolic Disease

16 July 2024

published in

1 reference

14 December 2017

volume

33

1 reference

14 December 2017

issue

6

1 reference

14 December 2017

page(s)

705-713

1 reference

Cloning, bacterial expression, and unique structure of adenosylhomocysteine hydrolase-like protein 1, or inositol 1,4,5-triphosphate receptor-binding protein from mouse kidney

14 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS10545-010-9171-X

Glycine N -methyltransferase deficiency: a new patient with a novel mutation

21 January 2018

1 reference

12 December 2020

Automated identification of putative methyltransferases from genomic open reading frames

1 reference

12 December 2020

S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy

1 reference

12 December 2020

S-adenosylhomocysteine hydrolase (AHCY) deficiency: two novel mutations with lethal outcome

1 reference

12 December 2020

IRBIT, a novel inositol 1,4,5-trisphosphate (IP3) receptor-binding protein, is released from the IP3 receptor upon IP3 binding to the receptor

1 reference

12 December 2020

Isozyme and DNA analysis of human S-adenosyl-L-homocysteine hydrolase (AHCY).

1 reference

12 December 2020

Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemia

1 reference

12 December 2020

S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism

1 reference

12 December 2020

The sulfur-containing amino acids: an overview

1 reference

12 December 2020

Identification of an S-adenosylhomocysteine hydrolase-like transcript induced during dendritic cell differentiation.

1 reference

12 December 2020

S-adenosylhomocysteine hydrolase deficiency in a 26-year-old man.

1 reference

12 December 2020

The mouse lethal nonagouti (a(x)) mutation deletes the S-adenosylhomocysteine hydrolase (Ahcy) gene

1 reference

12 December 2020

The cisterna magna septa: vestigial remnants of Blake's pouch and a potential new marker for normal development of the rhombencephalon

1 reference

12 December 2020

Identifiers

1 reference

Dimensions Publication ID

14 December 2017

1031856123

0 references

1 reference