Keyphrases
Hexosaminidase A
91%
Tay-Sachs Disease
78%
Tay-Sachs
57%
β-hexosaminidase
44%
Schizophrenia
41%
Ashkenazi Jews
40%
GM2 Gangliosidosis
33%
Ashkenazi
23%
Israeli
23%
Bipolar Disorder
21%
Hexosaminidase B
20%
Jewish
18%
Schizophrenic Patients
18%
Fetus
18%
Gangliosidosis
18%
Spinal muscular Atrophy
16%
Compound Heterozygous mutation
16%
Genotype
15%
Late-onset
15%
HEXA Gene
14%
Moroccan
14%
Jewish Population
14%
Leukocytes
14%
Skin Fibroblasts
13%
Jewish Patients
13%
Cultured Skin
12%
Heat-labile
12%
KCNN3
12%
CAG Repeat
12%
Gangliosides
12%
New mutation
12%
Jewish Family
11%
Schizophrenia Symptoms
10%
Moroccan Jews
10%
Fibroblasts
10%
Isozymes
10%
Prenatal Diagnosis
10%
Haplotype Analysis
10%
Point mutation
9%
Adult Form
9%
Charcot-Marie-Tooth Disease
8%
Late Infantile
8%
β-N-acetylhexosaminidase
8%
Sulforhodamine 101
8%
Association Study
8%
Amniotic Fluid Cells
8%
Duplication
8%
Pyrimethamine
8%
Quantitative PCR
8%
Polymorphism
8%
Biochemistry, Genetics and Molecular Biology
Hexosaminidase
100%
Tay-Sachs Disease
84%
GM2 Gangliosidoses
32%
Allele
30%
HEXA
29%
Fibroblast
23%
Exon
21%
Genetics
16%
Ganglioside
16%
Enzyme
15%
Gangliosidosis
12%
Leukocyte
12%
Haplotype
10%
Isoenzyme
10%
Codon
10%
Point Mutation
9%
GM1
8%
Homozygote
7%
Compound Heterozygosity
7%
Precursor
6%
Real-Time Polymerase Chain Reaction
6%
Genotyping
6%
Adrenergic Receptor
6%
Prevalence
6%
Arginine
6%
Exon Skipping
6%
Immunodiffusion
5%
