(Q45569163)

14 December 2017

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

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14 December 2017

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9

S Harvey Mudd

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14 December 2017

Randall Grubbs

1

1 reference

14 December 2017

Oliver Vugrek

2

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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

18 September 2010

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Journal of Inherited Metabolic Disease

14 December 2017

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14 December 2017

33

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14 December 2017

6

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14 December 2017

705-713

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https://scigraph.springernature.com/pub.10.1007/s10545-010-9171-x

14 December 2017

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cites work

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

1 reference

Crossref

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

10.1007/S10545-010-9171-X

Identifiers

DOI

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Dimensions Publication ID

14 December 2017

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1 reference