Keyphrases
Hereditary Myopathy
100%
Mitochondrial Processes
100%
Transcriptome
27%
Adult-onset
18%
Primary Function
9%
Expression Profile
9%
Expression Pattern
9%
Jewish
9%
Founder mutation
9%
Pathophysiology
9%
Statistical Methods
9%
Morphological Analysis
9%
Pathogenic Mechanism
9%
Differentially Expressed Genes
9%
Student's T-test
9%
Confocal Microscopy
9%
Myopathy
9%
Early Onset
9%
Genome-wide Expression
9%
Profile Data
9%
Sialic Acid
9%
Persian
9%
Gene chip
9%
Disease Mechanisms
9%
Expression Microarray
9%
Histological Changes
9%
Slowly Progressive
9%
Video Rate
9%
Mitochondrial Pathway
9%
Pathway Dysregulation
9%
Limb-girdle
9%
Muscle Disease
9%
Differentially Expressed mRNAs (DEmRNAs)
9%
Distal Myopathy
9%
Slow Evolution
9%
Proximal Myopathy
9%
Onset Condition
9%
Idiopathic Inflammatory Myopathies
9%
Biochemistry, Genetics and Molecular Biology
Transcriptome
100%
Enzyme
33%
Morphology
33%
Microarrays
33%
Mitochondrion
33%
Anabolism
33%
Confocal Microscopy
33%
GNE (Gene)
33%
Student's t-Test
33%
Genomics
33%
Sialic Acid
33%
Medicine and Dentistry
Myopathy
100%
Transcriptome
21%
Disease
14%
Limb
7%
Student T Test
7%
Pathophysiology
7%
Morphology
7%
Confocal Microscopy
7%
Mitochondrion
7%
Muscle Disease
7%
Sialic Acid
7%
Neuroscience
Muscle Disorder
100%
Transcriptome
20%
Mitochondrion
6%
Anabolism
6%
Confocal Microscopy
6%
Microarrays
6%
Sialic Acid
6%