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-Reference-Cited by-同舟云学术

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

Published:2001-12 Issue:4 Volume:74 Page:458-475
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Kovach Margaret J.,Waggoner Brook,Leal Suzanne M.,Gelber David,Khardori Romesh,Levenstien Mark A.,Shanks Christy A.,Gregg Gregory,Al-Lozi Muhammad T.,Miller Timothy,Rakowicz Wojtek,Lopate Glenn,Florence Juliane,Glosser Guila,Simmons Zachary,Morris John C.,Whyte Michael P.,Pestronk Alan,Kimonis Virginia E.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference59 articles.

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3. A novel autosomal dominant distal myopathy with early respiratory failure: Clinico-pathologic characteristics and exclusion of linkage to candidate genetic loci;Chinnery;Ann Neurol,2001

4. Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13. 1;Martinsson;Am J Hum Genet,1999

5. Autosomal dominant myopathy: Missense mutation (glu-706-to-lys) in the myosin heavy chain IIa gene;Martinsson;Proc Natl Acad Sci USA,2000

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