Mutation identification of Fabry disease in families with other lysosomal storage disorders.

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Mutation identification of Fabry disease in families with other lysosomal storage disorders.

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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name

Mutation identification of Fab ...... r lysosomal storage disorders.

@en

Mutation identification of Fab ...... r lysosomal storage disorders.

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label

Mutation identification of Fab ...... r lysosomal storage disorders.

@en

Mutation identification of Fab ...... r lysosomal storage disorders.

@nl

prefLabel

Mutation identification of Fab ...... r lysosomal storage disorders.

@en

Mutation identification of Fab ...... r lysosomal storage disorders.

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P1476

Mutation identification of Fab ...... er lysosomal storage disorders

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P2093

D Antuzzi

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F Bertola

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F Giurdanella

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L Fania

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M Filocamo

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S Lualdi

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P2860

Clinical manifestations of Fabry disease in children: data from the Fabry Outcome Survey.

Fabry disease and the skin: data from FOS, the Fabry outcome survey.

Expression of the disease on female carriers of X-linked lysosomal disorders: a brief review.

Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study.

Prevalence of lysosomal storage disorders.

High incidence of later-onset fabry disease revealed by newborn screening

The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK

Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males

Fucosidosis with angiokeratoma. Immunohistochemical & electronmicroscopic study of a new case and literature review.

Fabry disease in children and the effects of enzyme replacement treatment.

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281-285

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scholarly article

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10.1111/CGE.12071

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2012-12-28T00:00:00Z

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233847837

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23210910

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