Report Dominant Intermediate Charcot-Marie-Tooth Type C Maps to Chromosome 1p34-p35
Frontiers | A network of RNA and protein interactions in Fronto Temporal Dementia
Frontiers | Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants
Impact of Autosomal Recessive Juvenile Parkinson's Disease Mutations on the Structure and Interactions of the Parkin Ubiquitin
Animal models and therapeutic prospects for CharcotMarieTooth disease
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Localization of mitofusin 2 (MFN2) mutations. Previously reported... | Download Scientific Diagram
Genetic analyses of early-onset Alzheimer's disease using next generation sequencing | Scientific Reports
MFN2 mutation distribution and genotype/ phenotype correlation in Charcot–Marie– Tooth type 2
Genetics of Early-Onset Alzheimer Dementia
![PDF] Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD–ALS spectrum disorders | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/303d8d4e7cfb8f3ef8f2998e975c78d038f80b8f/2-Table1-1.png "PDF] Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD–ALS spectrum disorders | Semantic Scholar")
PDF] Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD–ALS spectrum disorders | Semantic Scholar
Binding Partners of Alzheimer's Disease Proteins: Are They Physiologically Relevant?
Disease-Modifying Therapies in Frontotemporal Lobar Degeneration
MolGen - Global solutions provider of innovative DNA / RNA extraction
MolGen - Global solutions provider of innovative DNA / RNA extraction
PDF) Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40 | Christine Van Broeckhoven - Academia.edu
Properties and units in the clinical laboratory sciences part XXIV. Properties and units in clinical molecular genetics (IUPAC Technical Report) in: Pure and Applied Chemistry Volume 90 Issue 7 (2018)
Review Article: Genetics of Alzheimer Disease
High frequency of SH3TC2 mutations in Czech HMSN I patients
Molecular genetics of Dravet syndrome
PS mutations. Schematic representation of PS1, the most frequently... | Download Scientific Diagram
Disease‐related mutations among Caribbean Hispanics with familial dementia - Lee - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
PDF) novoSNP, a novel computational tool for sequence variation discovery | Christine Van Broeckhoven - Academia.edu
Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia family
Deletion of lrrk2 causes early developmental abnormalities and age-dependent increase of monoamine catabolism in the zebrafish brain | PLOS Genetics
IJMS | Free Full-Text | Hereditary and Sporadic Forms of Aβ-Cerebrovascular Amyloidosis and Relevant Transgenic Mouse Models
PDF) Locus-Specific Mutation Databases for Neurodegenerative Brain Diseases
Mechanisms of long noncoding RNA function in development and disease – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub.
