DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» SGSH
SGSH
SUMF1 Enhances Sulfatase Activities in Vivo in Five Sulfatase Deficiencies
Bioinformatics Classification of Mutations in Patients with Mucopolysaccharidosis IIIA
EGL Test Description
Mucopolysaccharidosis Type IIIA, and a Child with One SGSH Mutation and One GNS Mutation Is a Carrier
Mucopolysaccharidosis I Diagnosing MPS I
Discover Dysplasias Gene Panel
Clinica Chimica Acta 436 (2014) 112–120
Brain-Specific Functional Relationship Networks Inform Autism Spectrum
Storage Disorders
Download PDF of Article
Gen Genetic Test Genetic Test Subjectkey (NDAR GUID)
Oxidized Phospholipids Regulate Amino Acid Metabolism Through MTHFD2 to Facilitate Nucleotide Release in Endothelial Cells
Lysosomal Storage Disorders
A Multiparametric Computational Algorithm for Comprehensive Assessment of Genetic Mutations in Mucopolysaccharidosis Type IIIA (Sanfilippo Syndrome)
Aagab S00002 Aars S00003 Aars2 S00004 Aass S02483
Emerging Approaches for Fluorescence-Based Newborn Screening of Mucopolysaccharidoses
High and Prolonged Sulfamidase Secretion by the Liver of MPS-IIIA Mice Following Hydrodynamic Tail Vein Delivery of Antibiotic-Free Pfar4 Plasmid Vector
Supplementary Tables 1-18 Contain the Predictive Signatures Determined for Each AML Subgroup Using Prediction Analysis for Microarrays (PAM)
Top View
Sanfilippo Syndrome
Lineage-Specific Effector Signatures of Invariant NKT Cells Are Shared Amongst Δγ T, Innate Lymphoid, and Th Cells
Natural Disease History and Characterisation of SUMF1
CPT Code and Price List 2021 CPT Codes
Bucy Syndrome Associated with a Recessive Variant in HGSNAT in Two Siblings with Mucopolysaccharidosis Type IIIC (Sanfilippo C)
Pioneering Gene Therapies for Rare Cns Diseases
Lysosomal Storage Disease Panel by Next-Generation Sequencing
SGSH Gene N-Sulfoglucosamine Sulfohydrolase
SULF1 and SULF2 Roger S Holmes* Griffith Institute for Drug Discovery and School of Natural Sciences, Griffith University, Nathan, QLD, Australia
Comparative and Evolutionary Studies of Vertebrate Arylsulfatase B
(12) Patent Application Publication (10) Pub. No.: US 2010/0068.195 A1 VELLARD Et Al
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
1 Pharmacological Chaperones for the Mucopolysaccharidoses Juan
Highlights on Genomics Applications for Lysosomal Storage Diseases
Oncogenic Effects of Germline Mutations in Lysosomal Storage Disease Genes
Molecular-Genetic Characterization of Ukrainian Patients with Mucopolysaccharidosis IIIA: Identification of Three New Mutations in the Heparan-N-Sulfatase Gene N
Stem Cell Potency and the Ability to Contribute to Chimeric Organisms
Identification and in Silico Analysis of GALNS Mutations Causing Morquio a Syndrome in Eight Consanguineous Families