Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype
Publication year
1996Source
Journal of Medical Genetics, 33, (1996), pp. 458-464ISSN
Publication type
Article / Letter to editor

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Organization
Neurology
Journal title
Journal of Medical Genetics
Volume
vol. 33
Page start
p. 458
Page end
p. 464
Subject
Clinical description and delineation of genetic syndromes; Inborn errors of metabolism; Klinische beschrijving en moleculaire definiëring van genetische syndromen; StofwisselingsziektenThis item appears in the following Collection(s)
- Academic publications [232014]
- Faculty of Medical Sciences [89012]
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