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Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle α-actin (ACTA1) gene |
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Titel: |
Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle α-actin (ACTA1) gene |
Auteur: |
Jungbluth, H Sewry, C.A Brown, S.C Nowak, K.J Laing, N.G Wallgren-Pettersson, C Pelin, K Manzur, A.Y Mercuri, E Dubowitz, V Muntoni, F |
Verschenen in: |
Neuromuscular disorders |
Paginering: |
Jaargang 11 (2001) nr. 1 pagina's 6 p. |
Jaar: |
2001 |
Inhoud: |
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Uitgever: |
Elsevier Science B.V. |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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