Home
About
Overview
Sharing Data
ORCID
Help
History (10)
AAV-Genome Population Sequencing of Vectors Packaging CRISPR Components Reveals Design-Influenced Heterogeneity.
Anti-CRISPR AcrIIA5 Potently Inhibits All Cas9 Homologs Used for Genome Editing.
Alcohol consumption and cardiovascular mortality among U.S. adults, 1987 to 2002.
Conlin, Frederick
AAV-Mediated Gene Therapy for Glycosphingolipid Biosynthesis Deficiencies.
See All 10 Pages
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
AAV-Mediated Gene Therapy for Glycosphingolipid Biosynthesis Deficiencies.
Yang H, Brown RH, Wang D, Strauss KA, Gao G. AAV-Mediated Gene Therapy for Glycosphingolipid Biosynthesis Deficiencies. Trends Mol Med. 2021 06; 27(6):520-523.
View in:
PubMed
subject areas
Dependovirus
Epilepsy
Genetic Therapy
Genetic Vectors
Hereditary Sensory and Autonomic Neuropathies
Humans
Phenotype
Recombinant Proteins
Sialyltransferases
Spastic Paraplegia, Hereditary
authors with profiles
Dan Wang PhD
Kevin Strauss MD
Robert H Brown MD, DPhil
Guangping Gao PhD