Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

To characterize the expression of distinct fragments of laminin alpha2 chain in patients with partial laminin alpha2 chain deficiency and variable clinical severity.
OriginalsprogEngelsk
TidsskriftNeurology
Vol/bind51
Udgave nummer1
Sider (fra-til)94-100
Antal sider7
ISSN0028-3878
StatusUdgivet - 1 jul. 1998

ID: 34325844