IJMS | Free Full-Text | Abnormal Pre-mRNA Splicing in Exonic Fabry Disease-Causing GLA Mutations
Identification of a novel loss-of-function mutation of the GLA gene in a Chinese Han family with Fabry disease | BMC Medical Genetics | Full Text
GLA Gene - GeneCards | AGAL Protein | AGAL Antibody
IJMS | Free Full-Text | Using CRISPR/Cas9-Mediated GLA Gene Knockout as an In Vitro Drug Screening Model for Fabry Disease
Alignment of gene sequences. Portion of the sequence of exon 2 of the... | Download Scientific Diagram
Cureus | New Mutation That Causes Fabry Disease Found in GLA Gene
New mutations in the GLA gene in Brazilian families with Fabry disease | Journal of Human Genetics
Genotyping of the GLA gene in heterozygous females: A. Patient CB, a... | Download Scientific Diagram
Three-dimensional structure of GLA gene and location of mutations... | Download Scientific Diagram
IJMS | Free Full-Text | Human α-Galactosidase A Mutants: Priceless Tools to Develop Novel Therapies for Fabry Disease
Alignment of gene sequences. Portion of the sequence of exon 3 of the... | Download Scientific Diagram
IJMS | Free Full-Text | Drug Repositioning for Fabry Disease: Acetylsalicylic Acid Potentiates the Stabilization of Lysosomal Alpha-Galactosidase by Pharmacological Chaperones
Fabry disease - Wikipedia
GLA/alpha-Galactosidase A Gene Sequence, Family, Fuction and Expression Information | Sino Biological
New Mutation Causing Fabry Found in GLA Gene, Case Study Reports
A deficiency of alpha-galactosidase A due to mutations in the GLA gene is responsible for Fabry disease | Disease, Ocular, Disorders
Proteostasis regulators modulate proteasomal activity and gene expression to attenuate multiple phenotypes in Fabry disease
Fabry Type 2 Likely Caused by A143T Mutation in GLA Gene, Study Says
File:Matrix Gla protein gene.jpg - Wikimedia Commons
SciELO - Brasil - GLA Gene Mutation in Hypertrophic Cardiomyopathy with a New Variant Description: Is it Fabry's Disease? GLA Gene Mutation in Hypertrophic Cardiomyopathy with a New Variant Description: Is it
Functional and pharmacological evaluation of novel GLA variants in Fabry disease identifies six (two de novo) causative mutations and two amenable variants to the chaperone DGJ - ScienceDirect
Novel α-galactosidase A gene mutation in a Chinese Fabry disease family: A case report
Mutations of the GLA Gene in Young Patients With Stroke | Stroke
Late diagnosis of Fabry disease caused by a de novo mutation in a patient with end stage renal disease | BMC Research Notes | Full Text
Identification of a novel loss-of-function mutation of the GLA gene in a Chinese Han family with Fabry disease | BMC Medical Genetics | Full Text
