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5 in total

Review 1. Myelin gene dosage and mutation in the hereditary motor and sensory neuropathies: a review.

Authors: G Nicholson
Journal: J Neurol Neurosurg Psychiatry Date: 1995-05 Impact factor: 10.154

2. Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.

Authors: F L Mastaglia; K J Nowak; R Stell; B A Phillips; J E Edmondston; S M Dorosz; S D Wilton; J Hallmayer; B A Kakulas; N G Laing
Journal: J Neurol Neurosurg Psychiatry Date: 1999-08 Impact factor: 10.154

3. Mutation analysis of MFN2, GJB1, MPZ and PMP22 in Italian patients with axonal Charcot-Marie-Tooth disease.

Authors: Giorgia Bergamin; Francesca Boaretto; Chiara Briani; Elena Pegoraro; Mario Cacciavillani; Andrea Martinuzzi; Maria Muglia; Andrea Vettori; Giovanni Vazza; Maria Luisa Mostacciuolo
Journal: Neuromolecular Med Date: 2014-05-13 Impact factor: 3.843

4. Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B.

Authors: E Nelis; V Timmerman; P De Jonghe; L Muylle; J J Martin; C Van Broeckhoven
Journal: J Med Genet Date: 1994-10 Impact factor: 6.318

5. Correlations between clinical, electrophysiological and genetic findings in hereditary motor and sensory neuropathy type I (HMSN I).

Authors: L Leonardis; J Zidar; J Trontelj; B Peterlin
Journal: Pflugers Arch Date: 1996 Impact factor: 3.657

5 in total