Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy.

Wallgren-Pettersson, C; Pelin, K; Hilpelä, P; Donner, K; Porfirio, B; Graziano, C; Swoboda, K J; Fardeau, M; Urtizberea, J A; Muntoni, F; Sewry, C; Dubowitz, V; Iannaccone, S; Minetti, C; Pedemonte, M; Seri, M; Cusano, R; Lammens, M; Castagna-Sloane, A; Beggs, A H; Laing, N G; de la Chapelle, A

Wallgren-Pettersson, C; Pelin, K; Hilpelä, P; Donner, K; Porfirio, B; Graziano, C; Swoboda, K J; Fardeau, M; Urtizberea, J A; Muntoni, F; Sewry, C; Dubowitz, V; Iannaccone, S; Minetti, C; Pedemonte, M; Seri, M; Cusano, R; Lammens, M; Castagna-Sloane, A; Beggs, A H; Laing, N G; de la Chapelle, A.

Affiliation

Wallgren-Pettersson C; Department of Medical Genetics, University of Helsinki, and The Folkhälsan Institute of Genetics, Finland. carina.wallgren@helsinki.fi

Neuromuscul Disord ; 9(8): 564-72, 1999 Dec.

Article in En | MEDLINE | ID: mdl-10619714

Subject(s)

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Genetic Variation / Myopathies, Nemaline / Genes, Recessive Limits: Child / Child, preschool / Humans / Infant Language: En Journal: Neuromuscul Disord Journal subject: NEUROLOGIA Year: 1999 Document type: Article Affiliation country: Country of publication:

Search on Google

Add to My VHL

XML

PubMed Links