Molecular analysis in a GALNS study cohort of 15 Tunisian patients: description of a novel mutation

BACKGROUND: Mucopolysaccharidosis type IVA (MPS IVA) is an autosomal recessive disease caused by the deficiency of the lysosomal enzyme N-acetylgalactosamine-6-sulfate sulfatase (GALNS). The purpose of this study was to analyze the GALNS mutations and the haplotypes associated. METHODS: Mutation scr...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Diagn Pathol
Autors principals: Chkioua, Latifa, Khedhiri, Souhir, Hafsi, Hind, Grissa, Oussama, Ben Turkia, Hadhami, Miled, Abdelhedi, Laradi, Sandrine, Froissart, Roseline, Alif, Najat
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2016
Matèries:
Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4912732/
https://ncbi.nlm.nih.gov/pubmed/27317439
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13000-016-0498-y
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars