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Neuromuscular Disorders, 2014
Mutations affecting skeletal muscle isoforms of the tropomyosin genes may cause nemaline myopathy (NM), cap myopathy, core-rod myopathy, congenital fibre-type disproportion, core-rod myopathy, distal arthrogryposes and Escobar syndrome. Here we correlate the clinical picture of these diseases with novel (16) and previously reported (31) mutations of ...
M. Marttila +39 more
openaire +1 more source
Mutations affecting skeletal muscle isoforms of the tropomyosin genes may cause nemaline myopathy (NM), cap myopathy, core-rod myopathy, congenital fibre-type disproportion, core-rod myopathy, distal arthrogryposes and Escobar syndrome. Here we correlate the clinical picture of these diseases with novel (16) and previously reported (31) mutations of ...
M. Marttila +39 more
openaire +1 more source
2017
Il contributo propone una rassegna ordinata delle decisioni giurisprudenziali sull'art. 271 c.p.p.
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Il contributo propone una rassegna ordinata delle decisioni giurisprudenziali sull'art. 271 c.p.p.
openaire +1 more source

