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ACTA1
LE WE PMID CA
ACTA113501ACTA1

ACTA1

Congenital fiber type disproportion

SEPN1

TPM3 Tropomyosin3

Tropomyosin

2010  
1
Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion.
[19953533] Hum Mutat 31(2): 176-83 (2010)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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