Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene.

Creators: FIORILLO, CHIARA; MINETTI, CARLO; Brisca G; Cassandrini D; Scapolan S; Astrea G; Valle M; Scuderi F; Trucco F; Natali A; Magnano G; Gazzerro E; Arca M; Santorelli FM; Bruno C.

Others:: Fiorillo, Chiara; Brisca, G; Cassandrini, D; Scapolan, S; Astrea, G; Valle, M; Scuderi, F; Trucco, F; Natali, A; Magnano, G; Gazzerro, E; Minetti, Carlo; Arca, M; Santorelli, Fm; Bruno, C.

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