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Search Results - Löschl, Beate
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Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophy
by
Berger, Johannes
,
Löschl, Beate
,
Bernheimer, Hanno
,
Lugowska, Agnieszka
,
Tylki-Szymanska, Anna
,
Gieselmann, Volkmar
,
Molzer, Brunhilde
Published in
American journal of medical genetics
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American Journal Of Medical Genetics
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Adult
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Alleles
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Arylsulfatase A Mutations
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Arysulfatase A Mutations
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Austria
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Cerebroside-Sulfatase - Deficiency
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Cerebroside-Sulfatase - Genetics
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Child
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Child, Preschool
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Female
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Genotype-Phenotype Correlation
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Genotype‐Phenotype Correlation
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Humans
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Leukodystrophy, Metachromatic - Genetics
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Male
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Metachromatic Leukodystrophy
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Mutation
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Phenotype
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Poland
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Polymerase Chain Reaction
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Wiley-Blackwell Journals (Backfile Content)
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Wiley Online Library All Journals
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Wiley-Blackwell Read & Publish Collection
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