Biochemistry, Genetics and Molecular Biology
Genetic Disorder
100%
Mutant Protein
100%
Gene Deletion
100%
Point Mutation
100%
Transmembrane Domain
100%
Missense Mutation
100%
Genotype Phenotype Correlation
100%
Pelizaeus-Merzbacher Disease
100%
Medicine and Dentistry
DeJerine-Sottas Disease
100%
Disease
66%
Spasticity
33%
In Vitro
33%
Endoplasmic reticulum
33%
Limb
33%
Gene Deletion
33%
Bladder
33%
Genetic Disorder
33%
Point Mutation
33%
Cognitive Defect
33%
Central Nervous System
33%
Missense Mutation
33%
Genotype Phenotype Correlation
33%
Mutant Protein
33%
Myelin Deficiency
33%
Pelizaeus Merzbacher Disease
33%
Proteolipid Protein
33%
Keyphrases
Novel mutation
100%
PLP1
100%
Hereditary Spastic Paraplegia
100%
Spastic Paraplegia Type 2
100%
Endoplasmic Reticulum
14%
Mutant Protein
14%
Central Nervous System
14%
Cognitive Impairment
14%
Genetic Disease
14%
Point mutation
14%
Transmembrane Domain
14%
Missense mutation
14%
Spastic
14%
Genotype-phenotype Correlation
14%
Related Disorders
14%
Urinary Bladder
14%
Duplication
14%
Nystagmus
14%
Variable Expressivity
14%
ARGENTINA
14%
Pelizaeus-Merzbacher Disease
14%
Whole Gene Deletion
14%
Limb Spasticity
14%
Dysmyelination
14%
Neuroscience
Hereditary Spastic Paraplegia
100%
Cognitive Disorders
33%
Central Nervous System
33%
In Vitro
33%
Mutant Protein
33%
Point Mutation
33%
Missense Mutation
33%
Gene Deletion
33%
Proteolipid Protein
33%
Endoplasmic Reticulum
33%