Mutations in TPM3 are a common cause of congenital fiber type disproportion
Annals of Neurology2008Vol. 63(3), pp. 329–337
Citations Over TimeTop 10% of 2008 papers
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, Annick Labarre‐Vila, Nicole Monnier, Nigel G. Laing, Kathryn N. North
Abstract
Mutation of TPM3 is the most common cause of CFTD reported to date.
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