Margaret J. Kovach

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

Giles D. Watts, Jill Wymer, Margaret J. Kovach et al. · Nature Genetics · 2004 · 1.4K citations · Full text

Mutant Valosin-containing Protein, Alzheimer's Disease, Inclusion Body Myopathy +9

Chloroplast DNA sequence utility for the lowest phylogenetic and phylogeographic inferences in angiosperms: The tortoise and the hare IV

Joey Shaw, Hayden L. Shafer, Opal Rayne Leonard et al. · American Journal of Botany · 2014 · 397 citations · Full text

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

Margaret J. Kovach, Brook Waggoner, Suzanne M. Leal et al. · Molecular Genetics and Metabolism · 2001 · 197 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +12

Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone

Virginia Kimonis, Margaret J. Kovach, Brook Waggoner et al. · Genetics in Medicine · 2000 · 140 citations · Full text

Unique Family, Mendelian Disorder, Genetic Disorder +11

A Unique Point Mutation in the PMP22 Gene Is Associated with Charcot-Marie-Tooth Disease and Deafness

Margaret J. Kovach, Jing‐Ping Lin, Simeon A. Boyadjiev et al. · The American Journal of Human Genetics · 1999 · 83 citations · Full text

Mendelian Disorder, Genetic Disorder, Pmp22 Gene Is +8