Genetic and clinical aspects of Charcot-Marie-Too... [Clin Genet. 1974] - PubMed

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Sex-linked recessive inheritance in Charcot-Marie-tooth disease with partial clinical manifestations in female carriers. [Hum Genet. 1980]
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Review Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: delineation of the clinical features and review of the literature. [Am J Med Genet. 2002]
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Kovach MJ, Campbell KC, Herman K, Waggoner B, Gelber D, Hughes LF, Kimonis VE. Am J Med Genet. 2002 Apr 1; 108(4):295-303.

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Cited by 76 PubMed Central articles

Molecular genetics of charcot-marie-tooth disease: from genes to genomes. [Mol Syndromol. 2012]
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Charcot-Marie-Tooth type 2B disease-causing RAB7A mutant proteins show altered interaction with the neuronal intermediate filament peripherin. [Acta Neuropathol. 2013]
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Cogli L, Progida C, Thomas CL, Spencer-Dene B, Donno C, Schiavo G, Bucci C. Acta Neuropathol. 2013 Feb; 125(2):257-72. Epub 2012 Nov 23.
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Myelin is dependent on the Charcot-Marie-Tooth Type 4H disease culprit protein FRABIN/FGD4 in Schwann cells.
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Genetic and clinical aspects of Charcot-Marie-Tooth's disease.
Genetic and clinical aspects of Charcot-Marie-Tooth's disease.
Clin Genet. 1974 ;6(2):98-118.

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