Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia (Q28212105)
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scientific article (publication date: December 2001)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia |
scientific article (publication date: December 2001) |
Statements
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia (English)
M J Kovach
B Waggoner
S M Leal
D Gelber
R Khardori
M A Levenstien
C A Shanks
G Gregg
M T Al-Lozi
T Miller
W Rakowicz
G Lopate
J Florence
G Glosser
Z Simmons
J C Morris
M P Whyte
A Pestronk
V E Kimonis
December 2001
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