A new mutation found in newborn screening for Fabry disease evaluated by plasma globotriaosylsphingosine levels

A pilot study of newborn screening for Fabry disease was performed in Okinawa, Japan. A total of 2,443 neonates were screened using dried blood spot samples over 7 years starting in 2007. Of 13 neonates determined to have low α-galactosidase A (GLA) activity, one boy had a new missense mutation, p.G...

Descripción completa

Detalles Bibliográficos
Autores principales: Chinen, Yasutsugu, Nakamura, Sadao, Yoshida, Tomohide, Maruyama, Hiroki, Nakamura, Kimitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5311055/
https://www.ncbi.nlm.nih.gov/pubmed/28224042
http://dx.doi.org/10.1038/hgv.2017.2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5311055/
https://www.ncbi.nlm.nih.gov/pubmed/28224042
http://dx.doi.org/10.1038/hgv.2017.2

Ejemplares similares