(Q44115114)
Statements
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Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy (English)
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Iannaccone ST
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Swoboda KJ
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Wattanasirichaigoon D
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Takada F
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Tong HQ
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Lip V
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Wallgren-Pettersson C
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Laing NG
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Beggs AH
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1 August 2002
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59
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4
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613-617
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Identifiers
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