Biochemistry, Genetics and Molecular Biology
Phenotypic Heterogeneity
100%
X Chromosome
100%
Genetic Counseling
100%
Mouse
100%
Exome Sequencing
100%
Phosphotransferase
100%
Kinase
100%
Necroptosis
100%
Mosaicism
100%
Genetic Screening
100%
Genetics
50%
Mental Retardation
50%
DNA Binding Domain
50%
Heterozygosity
50%
Synapsin I
50%
Oxygenase
42%
Haplotype
14%
Amino Acids
14%
Cell Death
14%
Enzyme Activity
14%
Magnetism
14%
Primary Cell
14%
Lipidomics
14%
Whole Genome Sequencing
14%
Neuroscience
Necroptosis
100%
Spectrum Disorder
100%
Mixed Lineage Kinase
100%
Oxygenase
42%
Neurodegenerative Disorder
28%
Fatty Acids
28%
Central Nervous System
14%
Nervous System
14%
Enzyme Activity
14%
Cell Death
14%
Cerebellum
14%
Haplotype
14%
Ataxia
14%
Paresis
14%
Dysarthria
14%
Neurodegeneration
14%
Primary Progressive Multiple Sclerosis
14%
Whole Genome Sequencing
14%
Amino Acid
14%
Brainstem
14%
Magnetic Resonance Imaging
14%
Immunology and Microbiology
Lineages
100%
Necroptosis
100%
Primary Progressive Multiple Sclerosis
14%
Cerebellum
14%
Central Nervous System
14%
Nervous System
14%
Haplotype
14%
Enzyme Activity
14%
Cell Death
14%
Magnetic Resonance Imaging
14%
Whole Genome Sequencing
14%
