Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: Clinical and pathological variability within a kindred

Autor: Hutchinson, David O.1 dhutch@adhb.govt.nz, Charlton, Amanda2, Laing, Nigel G.3, Ilkovski, Biljana4, North, Kathryn N.4
Zdroj: Neuromuscular Disorders. Feb2006, Vol. 16 Issue 2, p113-121. 9p.
Databáze: Academic Search Ultimate
Externí odkaz: