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Novel fukutin mutations in limb-girdle muscular dystrophy type 2M with childhood onset. | LitMetric

Novel fukutin mutations in limb-girdle muscular dystrophy type 2M with childhood onset.

Neurol Genet

Institute of Human Genetics (M.S., B.Z., S.P.), Department of Neurology (J.Z., J.S.), and Department of Neuroradiology (P.H.), University Medical Center Göttingen; Department of Human Genetics (W.K.), University of Würzburg; and CeGaT GmbH und Praxis für Humangenetik (J.M.), Tübingen, Germany.

Published: August 2017

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524525PMC
http://dx.doi.org/10.1212/NXG.0000000000000167DOI Listing

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