Novel Mutation in the IDS Gene in Hunter Syndrome Associated with Severe Cardiac Lesions.

Subjects

Subjects :

Heart Defects, Congenital complications
Humans
Infant
Male
Mucopolysaccharidosis II complications
Glycoproteins genetics
Heart Defects, Congenital diagnosis
Heart Defects, Congenital genetics
Mucopolysaccharidosis II diagnosis
Mucopolysaccharidosis II genetics
Mutation

Details

Language :

English

ISSN :

1530-8561

Volume :

67

Issue :

3

Database :

MEDLINE

Journal :

Clinical chemistry

Publication Type :

Academic Journal

Accession number :

33674846

Full Text :

https://doi.org/10.1093/clinchem/hvaa334