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Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

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Title: Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
Authors: Watts GD; Division of Genetics, Children's Hospital Boston, Harvard Medical School, Boston, MA, USA., Thomasova D, Ramdeen SK, Fulchiero EC, Mehta SG, Drachman DA, Weihl CC, Jamrozik Z, Kwiecinski H, Kaminska A, Kimonis VE
Source: Clinical genetics [Clin Genet] 2007 Nov; Vol. 72 (5), pp. 420-6.
Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print Cited Medium: Print ISSN: 0009-9163 (Print) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
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  Data: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>0009-9163 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1111/j.1399-0004.2007.00887.x
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      – TitleFull: Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
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              M: 11
              Text: 2007 Nov
              Type: published
              Y: 2007
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