Biochemistry, Genetics and Molecular Biology
Autosomal Dominant Inheritance
58%
Candidate Gene
44%
Haplotype
33%
Proband
33%
Genetics
33%
Linkage Analysis
33%
Cell Adhesion
33%
GTPase-activating Protein
33%
Rho Family of GTPases
33%
Exon
33%
Cell Migration
33%
Exome
33%
Cytoskeleton
33%
Cell Polarity
33%
RNA Processing
33%
Autosomal Recessive Inheritance
33%
Cell Proliferation
33%
Organogenesis
33%
Actin
33%
Missense Mutation
33%
Nerve Cell Degeneration
33%
GTPase
33%
Gain of Function Mutation
33%
Limb Bud
33%
Human Development
33%
Chromosome 16q
33%
Haploinsufficiency
33%
Membrane Trafficking
33%
Motor Neuron
27%
Gene Linkage
22%
SOD1
22%
Notch Signaling Pathway
16%
Missense
16%
Transcription
16%
RNA Splicing
16%
Exome Sequencing
16%
TARDBP
16%
RNA
16%
Ligand Binding Domain
16%
Notch
16%
Gene Expression
16%
Messenger RNA
16%
Transient Transfection
16%
Lower Motor Neuron
16%
Amino Acid Substitution
16%
Leukocyte
16%
Dominant Inheritance
16%
HES1
16%
Downregulation
16%
Microsatellite Marker
11%
Neuroscience
Amyotrophic Lateral Sclerosis
100%
Frontotemporal Dementia
38%
Chromosome 16q
33%
RNA Processing
33%
Haplotype
18%
Nerve Cell Degeneration
16%
Missense Mutation
16%
Copper Zinc Superoxide Dismutase
13%
SOD1
9%
Microsatellite
8%
Neurodegenerative Disorder
8%
RNA Splicing
8%
RNA Binding Protein FUS
8%
Lower Motor Neuron
8%
Medicine and Dentistry
Sensorineural Hearing Loss
33%
Muscle Biopsy
33%
Clinical Feature
22%
Differential Diagnosis
22%
Centronuclear Myopathy
22%
Corpus Callosum Agenesis
22%
Immune Deficiency
11%
Hypopigmentation
11%
Respiratory Chain
11%
Cataract
11%
DeJerine-Sottas Disease
11%
Disorders of Mitochondrial Functions
11%
Trichrome
11%
Myocardial Disease
11%
Diseases
11%
