A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophy (Englisch)
- Neue Suche nach: Margoni, M.
- Neue Suche nach: Soli, F.
- Neue Suche nach: Sangalli, A.
- Neue Suche nach: Bellizzi, M.
- Neue Suche nach: Cecchini, E.
- Neue Suche nach: Buganza, M.
- Neue Suche nach: Margoni, M.
- Neue Suche nach: Soli, F.
- Neue Suche nach: Sangalli, A.
- Neue Suche nach: Bellizzi, M.
- Neue Suche nach: Cecchini, E.
- Neue Suche nach: Buganza, M.
In:
Journal of clinical neuroscience
;
43
;
175-177
;
2017
-
ISSN:
- Aufsatz (Zeitschrift) / Print
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Titel:A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophy
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Beteiligte:Margoni, M. ( Autor:in ) / Soli, F. ( Autor:in ) / Sangalli, A. ( Autor:in ) / Bellizzi, M. ( Autor:in ) / Cecchini, E. ( Autor:in ) / Buganza, M. ( Autor:in )
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Erschienen in:Journal of clinical neuroscience ; 43 ; 175-177
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Verlag:
- Neue Suche nach: Elsevier Science B.V., Amsterdam
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Erscheinungsdatum:01.01.2017
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Format / Umfang:3 pages
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ISSN:
-
Medientyp:Aufsatz (Zeitschrift)
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Format:Print
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Sprache:Englisch
- Neue Suche nach: 616.8
- Weitere Informationen zu Dewey Decimal Classification
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Klassifikation:
DDC: 616.8 -
Datenquelle:
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