(Q40015198)

16 September 2017

title

A novel fluorometric enzyme analysis method for Hunter syndrome using dried blood spots (English)

1 reference

16 September 2017

1

1 reference

16 September 2017

Carrie Graham

2

1 reference

16 September 2017

Qun Shi

3

1 reference

16 September 2017

Ramakrishna S Sista

4

1 reference

16 September 2017

Tong Wang

5

1 reference

16 September 2017

Allen E Eckhardt

6

1 reference

16 September 2017

Vamsee K Pamula

7

1 reference

16 September 2017

David S Millington

8

1 reference

16 September 2017

Deeksha S Bali

9

1 reference

16 September 2017

publication date

21 December 2011

1 reference

Molecular Genetics and Metabolism

16 September 2017

published in

1 reference

16 September 2017

volume

105

1 reference

16 September 2017

issue

3

1 reference

16 September 2017

page(s)

519-521

1 reference

Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome).

16 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2011.12.011

Multidisciplinary management of Hunter syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2011.12.011

Digital microfluidic platform for multiplexing enzyme assays: implications for lysosomal storage disease screening in newborns

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2011.12.011

Rapid, single-step assay for Hunter syndrome in dried blood spots using digital microfluidics

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2011.12.011

A fluorimetric enzyme assay for the diagnosis of MPS II (Hunter disease).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2011.12.011

10.1016/J.YMGME.2011.12.011

7 January 2021

Identifiers

DOI

1 reference

16 September 2017

1 reference