| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1097/00019052-199910000-00004 |
| P698 | PubMed publication ID | 10590887 |
| P50 | author | Nigel G Laing | Q56838398 |
| P2093 | author name string | Laing NG | |
| P433 | issue | 5 | |
| P304 | page(s) | 513-518 | |
| P577 | publication date | 1999-10-01 | |
| P1433 | published in | Current Opinion in Neurology | Q15716647 |
| P1476 | title | Inherited disorders of sarcomeric proteins | |
| P478 | volume | 12 |
| Q34174588 | Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation. |
| Q24684848 | Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene |
| Q33952706 | Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscle. |
| Q34284765 | Mice lacking skeletal muscle actin show reduced muscle strength and growth deficits and die during the neonatal period |
| Q34223063 | Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1). |
| Q34155789 | Nemaline cardiomyopathy in a young adult: an ultraimmunohistochemical study and review of the literature. |
| Q24537515 | Tropomyosin requires an intact N-terminal coiled coil to interact with tropomodulin |
| Q28201248 | p0071, a member of the armadillo multigene family, is a constituent of sarcomeric I-bands in human skeletal muscle |
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