Keyphrases
Iduronate 2-sulfatase Gene
71%
Photosystem II
71%
Indonesia
68%
Indonesian Patients
37%
6-pyruvoyltetrahydropterin Synthase
26%
Indonesian Population
26%
Novel Variation
22%
Iduronate-2-sulfatase
21%
Novel mutation
20%
Mucopolysaccharidosis IVA
17%
Exon 9
17%
Exon 4
17%
Exon 8
17%
Exon 5
17%
Silent mutation
17%
Exon
17%
Genotype
15%
Novel Variants
14%
Jakarta
14%
PTS Gene
13%
Healthy Individuals
13%
Deletion Variant
12%
Genotype-phenotype
11%
Rare Diseases
11%
Mutation Analysis
10%
Mutational Analysis
10%
Genome Analysis
10%
Protein Analysis
10%
Rural Areas
10%
Mutation Profiling
10%
Polymerase Chain Reaction
9%
Lysosomal Storage Disease
9%
Galactosamine
8%
Sulfatase
8%
Exon 6
8%
N-acetylation
8%
Causative Drugs
8%
Exon 7
8%
N-acetylgalactosamine
8%
Mutation Identification
8%
Exon 2
8%
Exon 3
8%
IDS Gene
8%
Meta-analysis
8%
Urban Indonesia
8%
Molecular Study
8%
DNA Quality
8%
Thalassemia
8%
West Java
8%
Transfusion-dependent Thalassemia
8%
Biochemistry, Genetics and Molecular Biology
Exon
100%
Mucopolysaccharidosis
82%
Iduronate-2-Sulfatase
71%
Synthase
26%
Genotyping
23%
Intron
21%
Silent Mutation
17%
Enzyme
15%
PTS (Gene)
12%
Protein Characterization
10%
Polymerase Chain Reaction
10%
Sulfate
10%
Exome
8%
Germline
8%
FUT2
8%
Germ Cell
8%
Galactosamine
8%
Sulfatase
8%
N-Acetylgalactosamine
8%
Morquio Syndrome
8%
Nonsense Mutation
6%
Amino Acids
6%
Hunter Syndrome
6%
Electrophoresis
6%
Genetics
6%
Dideoxynucleotide Sequencing
5%
Missense Mutation
5%
Genomics
5%
Peptide Sequence
5%
Gene Mutation
5%
Glycosaminoglycan
5%
Sapropterin
5%
Medicine and Dentistry
Exon
35%
Hunter Syndrome
26%
Iduronate 2 Sulfatase
26%
Silent Mutation
14%
Toxic Epidermal Necrolysis
8%
Meta-Analysis
8%
Carbamazepine
8%
Stevens-Johnson Syndrome
8%
Buccal Swab
8%
Neonate
8%
Diet Supplementation
8%
N Acetylgalactosamine
8%
Morquio Syndrome
8%
Mixed Gonadal Dysgenesis
8%
Sulfate
8%
Rare Disease
8%
Systematic Review
8%
Glycogen Storage Disease
8%
Exome Sequencing
8%
Prematurity
8%
Premature Labor
8%
Turner Syndrome
8%
Nutrition
6%
Glycogen Storage Disease Type IV
6%
Allele
5%
Nonsense Mutation
5%
