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

Author: Kovach M.J.   Waggoner B.   Leal S.M.   Gelber D.   Khardori R.   Levenstien M.A.   Shanks C.A.   Gregg G.   Al-Lozi M.T.   Miller T.   Rakowicz W.   Lopate G.   Florence J.   Glosser G.   Simmons Z.   Morris J.C.   Whyte M.P.   Pestronk A.   Kimonis V.E.  

Publisher: Academic Press

ISSN: 1096-7192

Source: Molecular Genetics and Metabolism, Vol.74, Iss.4, 2001-12, pp. : 458-475

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract