Mutations in <i>TPM3</i> are a common cause of congenital fiber type disproportion - Concepedia

Concepedia

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Mutations in <i>TPM3</i> are a common cause of congenital fiber type disproportion

168

Citations

26

References

2008

Year

Nigel F. Clarke, Hanna Kolski, Danielle E. Dye, Esther Lim, Robert L. Smith, Rakesh Patel, Michael Fahey, Rémi Bellance, Norma B. Romero, Edward S. Johnson,

Annals of Neurology

Abstract

Mutation of TPM3 is the most common cause of CFTD reported to date.

References

	Year	Citations

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