Biochemistry, Genetics and Molecular Biology
SMN2
100%
Nested Gene
53%
Newborn Screening
36%
Genetics
33%
Mutation
32%
Phenotype
29%
Childhood
29%
ATP1A3
27%
Motor Performance
23%
SMN1
22%
Age
19%
Protein
18%
Experience
16%
Spectrum
16%
Exome Sequencing
15%
Salbutamol
14%
Acetylcholine Receptor
14%
Short QT Syndrome
14%
Exome Sequencing
14%
Consensus
14%
Sample
13%
Clinical Trial
8%
Time
8%
Length
8%
Reduction (Chemistry)
8%
Skeletal Muscle
7%
Electric Potential
7%
Lean Body Weight
7%
Biomarker Study
7%
Cross Sectional Study
7%
Autosomal Recessive Inheritance
7%
Medicine and Dentistry
Spinal Muscular Atrophy
74%
Patient
57%
Gene
44%
Diagnosis
22%
Motor Performance
21%
Age
21%
Biological Marker
21%
Assessment
21%
Ceramide
14%
Phosphatase
14%
Lafora Disease
14%
Head and Neck Cancer
14%
Tensin
14%
Arthrogryposis
14%
Congenital Long-QT Syndrome
14%
Electroencephalogram
12%
Epilepsy
12%
Muscle
12%
Blood
11%
Survival Motor Neuron Protein
10%
Exome Sequencing
10%
Long QT Syndrome
9%
Phenotype
9%
Adult
9%
Serum
8%
Neuroimaging
8%
Diseases
7%
Disease Duration
7%
Lean Body Weight
7%
Laboratory
7%
Exon
7%
Clinical Feature
7%
Inpatient
6%
Therapeutic Procedure
6%
Neuromuscular Disease
6%
Cancer Epidemiology
5%
Plasma
5%
Autosomal Recessive Inheritance
5%
