HuGE Literature Finder
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Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene? Brain and behavior 2016 Mar e00451. Werheid Friederike, Azzedine Hamid, Zwerenz Eva, Bozkurt Ahmet, Moeller Marcus J, Lin Lilian, Mull Michael, Häusler Martin, Schulz Jörg B, Weis Joachim, Claeys Kristl |
The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy. Molecular genetics & genomic medicine 2014 Nov 2 (6): 522-9. DiVincenzo Christina, Elzinga Christopher D, Medeiros Adam C, Karbassi Izabela, Jones Jeremiah R, Evans Matthew C, Braastad Corey D, Bishop Crystal M, Jaremko Malgorzata, Wang Zhenyuan, Liaquat Khalida, Hoffman Carol A, York Michelle D, Batish Sat D, Lupski James R, Higgins Joseph |
Central nervous system abnormalities in patients with PMP22 gene mutations: a prospective study. Journal of neurology, neurosurgery, and psychiatry 2013 Apr 84 (4): 392-7. Chanson Jean-Baptiste, Echaniz-Laguna Andoni, Blanc Frédéric, Lacour Arnaud, Ballonzoli Laurent, Kremer Stéphane, Namer Izzie-Jacques, Lannes Béatrice, Tranchant Christine, Vermersch Patrick, de Seze Jérô |
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- Page last updated:Feb 07, 2023
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