Gene therapy for fabry disease: a review of the literature.
about
A snapshot of gene therapy in Latin AmericaCarboxyl-terminal truncations alter the activity of the human α-galactosidase ARole of endocytic uptake in transfection efficiency of solid lipid nanoparticles-based nonviral vectors.Gene therapy for lysosomal storage disorders: recent advances for metachromatic leukodystrophy and mucopolysaccaridosis I.GLA mutation as a risk factor for later life small vessel ischaemic disease.Cell therapy for diverse central nervous system disorders: inherited metabolic diseases and autism.Identification of a Missense Mutation in the α-galactosidase A Gene in a Chinese Family with Fabry Disease.
P2860
Q26998837-EF7CEB03-7931-4839-8717-D30AF9157CD8Q35125851-3E6E183B-0C85-48E8-A033-668E9B357BB6Q39043135-9D4FB0E6-4A93-4E79-95A5-48E066E6CA15Q39339697-BFB6D91C-5214-495B-ABF1-1396DA8DBCC2Q41856965-8674F433-2C9F-4C67-8867-EC4A9757DCCAQ49557884-0DA942D1-D086-4EF9-BE07-57E9A7B99EDBQ55379532-2A93A94F-51E6-4B04-92A4-6EC85EFC4106
P2860
Gene therapy for fabry disease: a review of the literature.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Gene therapy for fabry disease: a review of the literature.
@en
type
label
Gene therapy for fabry disease: a review of the literature.
@en
prefLabel
Gene therapy for fabry disease: a review of the literature.
@en
P2093
P2860
P1433
P1476
Gene therapy for fabry disease: a review of the literature.
@en
P2093
Alicia Rodríguez-Gascón
Aritz Perez Ruiz de Garibay
María Angeles Solinís
P2860
P2888
P304
P356
10.1007/S40259-013-0032-7
P577
2013-06-01T00:00:00Z