(Q28247784)

English

Hereditary inclusion body myopathy-linked p97/VCP mutations in the NH2 domain and the D1 ring modulate p97/VCP ATPase activity and D2 ring conformation

scientific article (publication date: August 2009)

Statements

Hereditary inclusion body myopathy-linked p97/VCP mutations in the NH2 domain and the D1 ring modulate p97/VCP ATPase activity and D2 ring conformation (English)
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Dalia Halawani
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Andréa C LeBlanc
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Marc J Servant
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Martin Latterich
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August 2009
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29
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16
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4484-94
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Identifiers

 
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