SGSH
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- 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