David Gelber

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Autosomal dominant myopathy, Paget disease of bone, and dementia constitute a unique disorder (MIM 605382). Here we describe the clinical, biochemical, radiological, and pathological characteristics(More)
A unique point mutation in the PMP22 gene is associated with Deafness, Charcot-MarieTooth and Antic~pation.V.E. Kimonis'. M.J. Kovach'. J-P. Lin2, S. Bovadiiev', K. Cam~bcll '. L. Mazzeo'. K.(More)