(Q28248133)

English

Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)

scientific article

Statements

Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2) (English)
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Homa Tajsharghi
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Monica Ohlsson
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Christopher Lindberg
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Anders Oldfors
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September 2007
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64
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9
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1334-8
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Identifiers

 
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