Hereditary Inclusion Body Myopathy
A new familial, autosomal dominant, myopathy and variant of hereditary inclusion body myopathy (HIBM) is described in 19 members of a large Swedish family followed in the Departments of Pediatrics, Genetics, and Pathology, Sahlgrenska University Hospital, Goteborg, Sweden.
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| Format: | Livre |
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Pediatric Neurology Briefs Publishers,
1998-09-01T00:00:00Z.
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A1234.567 |
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| Exemplaire 1 | Disponible |