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

GD Watts; D Thomasova; SK Ramdeen; EC Fulchiero; SG Mehta; DA Drachman; CC Weihl; Z Jamrozik; H Kwiecinski; A Kaminska; VE Kimonis

doi:10.1111/j.1399-0004.2007.00887.x

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

GD Watts, D Thomasova, SK Ramdeen, EC Fulchiero, SG Mehta, DA Drachman, CC Weihl, Z Jamrozik, H Kwiecinski, A Kaminska, VE Kimonis

Research output: Contribution to journal › Article

108 Citations (Scopus)

Original language	English
Pages (from-to)	420-426
Number of pages	7
Journal	Clinical Genetics
Volume	72
Issue number	5
DOIs	https://doi.org/10.1111/j.1399-0004.2007.00887.x
Publication status	Published - 2007

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10.1111/j.1399-0004.2007.00887.x

Cite this

@article{04c966ee66a448a8bf8dbfcdc1ac7eec,

title = "Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia",

author = "GD Watts and D Thomasova and SK Ramdeen and EC Fulchiero and SG Mehta and DA Drachman and CC Weihl and Z Jamrozik and H Kwiecinski and A Kaminska and VE Kimonis",

year = "2007",

doi = "10.1111/j.1399-0004.2007.00887.x",

language = "English",

volume = "72",

pages = "420--426",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley",

number = "5",

}

TY - JOUR

T1 - Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

AU - Watts, GD

AU - Thomasova, D

AU - Ramdeen, SK

AU - Fulchiero, EC

AU - Mehta, SG

AU - Drachman, DA

AU - Weihl, CC

AU - Jamrozik, Z

AU - Kwiecinski, H

AU - Kaminska, A

AU - Kimonis, VE

PY - 2007

Y1 - 2007

U2 - 10.1111/j.1399-0004.2007.00887.x

DO - 10.1111/j.1399-0004.2007.00887.x

M3 - Article

VL - 72

SP - 420

EP - 426

JO - Clinical Genetics

JF - Clinical Genetics

SN - 0009-9163

IS - 5

ER -