Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
To characterize the expression of distinct fragments of laminin alpha2 chain in patients with partial laminin alpha2 chain deficiency and variable clinical severity.
Originalsprog | Engelsk |
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Tidsskrift | Neurology |
Vol/bind | 51 |
Udgave nummer | 1 |
Sider (fra-til) | 94-100 |
Antal sider | 7 |
ISSN | 0028-3878 |
Status | Udgivet - 1 jul. 1998 |
ID: 34325844