Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy - Concepedia

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Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

225

Citations

27

References

2002

Year

Kati Donner, Miina Ollikainen, Maaret Ridanpää, H.‐J. Christen, Hans H. Goebel, Katarina Pelin, Carina Wallgren‐Pettersson

Neuromuscular Disorders

Rare CauseMedicineMolecular BiologyPathologyCytoskeletonCommon DiseasesNeuromuscular PathologyNemaline Myopathy

References

	Year	Citations

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