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Canavan disease: Diagnosis and molecular analysis
Reuben Matalon
Pediatrics
Research output
:
Contribution to journal
›
Article
›
peer-review
25
Scopus citations
Overview
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Dive into the research topics of 'Canavan disease: Diagnosis and molecular analysis'. Together they form a unique fingerprint.
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Keyphrases
Disease Diagnosis
100%
Canavan Disease
100%
Molecular Analysis
100%
Diagnostic Analysis
100%
Aspartoacylase
50%
Ashkenazi Jews
50%
Jewish Population
25%
N-acetylneuraminic Acid
25%
Autosomal Recessive
25%
Accurate Diagnosis
25%
Jewish
25%
Spongy Degeneration
25%
Carrier Screening
25%
Biochemical Markers
25%
Jewish Patients
25%
High Carrier Frequency
25%
Jews
25%
Pharmacology, Toxicology and Pharmaceutical Science
Canavan Disease
100%
Disease
50%
Aspartoacylase
50%
Prevalence
25%
N Acetylaspartic Acid
25%
Biochemical Marker
25%
Autosomal Recessive Disorder
25%
Biochemistry, Genetics and Molecular Biology
Canavan Disease
100%
Aspartoacylase
50%
Enzyme
25%
Prevalence
25%
Autosomal Recessive Disorder
25%