(Q42224934)

19 October 2017

title

Absence of hepatic molybdenum cofactor. An inborn error of metabolism associated with lens dislocation (English)

1 reference

19 October 2017

Beemer FA

1

1 reference

19 October 2017

Duran M

series ordinal

2

1 reference

19 October 2017

Wadman SK

series ordinal

3

1 reference

19 October 2017

Cats BP

series ordinal

4

1 reference

19 October 2017

publication date

1 April 1985

1 reference

Ophthalmic Paediatrics and Genetics

19 October 2017

published in

1 reference

19 October 2017

volume

5

1 reference

19 October 2017

issue

3

1 reference

19 October 2017

page(s)

191-195

1 reference

Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?

19 October 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F13816818509006133

Structural and metabolic relationship between the molybdenum cofactor and urothione

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816818509006133

Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816818509006133

Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816818509006133

10.3109/13816818509006133

21 January 2018

Identifiers

DOI

1 reference

19 October 2017

1 reference