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- The Neuronal Ceroid Lipofuscinosis Protein, Cln7, Regulates Neural Development from the Post-Synaptic Cell
- Next Generation Sequencing of 134 Children with Autism Spectrum Disorder and Regression
- A Novel MFSD8 Mutation in a Russian Patient with Neuronal Ceroid
- A Tailored Cln3q352x Mouse Model for Testing Therapeutic Interventions in CLN3 Batten Disease Logan Langin1,3, Tyler B
- Genome-Wide CNV Investigation Suggests a Role for Cadherin, Wnt, and P53 Pathways in Primary Open-Angle Glaucoma Valeria Lo Faro1,2, Jacoline B
- Novel Allelic Variants and Evidence for a Prevalent Mutation in URAT1 Causing Renal Hypouricemia: Biochemical, Genetics and Functional Analysis
- ARTICLE the Novel Neuronal Ceroid Lipofuscinosis Gene MFSD8 Encodes a Putative Lysosomal Transporter
- A Major Facilitator Superfamily Domain 8 Frameshift Variant in a Cat with Suspected Neuronal Ceroid Lipofuscinosis
- A Rare Homozygous MFSD8 Single-Base-Pair Deletion And
- “Atypical” Phenotypes of Neuronal Ceroid Lipofuscinosis
- (12) Patent Application Publication (10) Pub. No.: US 2015/0366997 A1 Guild Et Al
- Specific Alleles of CLN7/MFSD8, a Protein That Localizes To
- Specific Alleles of CLN7/MFSD8, a Protein That
- Transcriptomic Changes in the Pre-Implantation Uterus Highlight
- SFU Thesis Template Files
- Goat Anti-CLN2 / TPP1 Antibody Peptide-Affinity Purified Goat Antibody Catalog # Af1253a