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Neurology & Neurotherapy Open Access Journal

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Pervin Dincer

Pervin Dincer

Editorial Board Member
Hacettepe University Turkey Member since 2017

Biography

Dr. Pervin Dincer is a translational medicine investigator. Since 1994, she has been conducting translational research focused primarily on hereditary muscle diseases. She has identified the 4 causative genes for autosomal recessive limb-girdle muscular dystrophy (LGMD2) phenotypes including LGMD2K, LGMD2P, LGMD2Q and LGMD2R caused by mutation in POMT1, DAG1, PLEC1f and DES, respectively. In addition, she has recently identified a mutation in TOR1AIP1 encoding human LAP1 protein, as a cause of an autosomal recessively inherited myopathy with contractures and cardiomyopathy. Her studies consist of the identification of the causative gene through genetic linkage studies, homozygosity mapping and the elucidation of the molecular pathogenesis through functional studies.

Research Interests

Medical Biology Muscular dystrophy Cellular processes and functional prediction.

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