Authors: Ismailov, SM Fedotov, VP Dadali, EL Polyakov, AV Van Broeckhoven, C Ivanov, VI De Jonghe, P Timmerman, V Evgrafov, OV

Citation: Sm. Ismailov et al., A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21, EUR J HUM G, 9(8), 2001, pp. 646-650

Authors: Mersiyanova, IV Ismailov, SM Polyakov, AV Dadali, EL Fedotov, VP Nelis, E Lofgren, A Timmerman, V Van Broeckhoven, C Evgrafov, OV

Citation: Iv. Mersiyanova et al., Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32(GJB1) in Russian Charcot-Marie-Tooth neuropathy patients (vol 15, pg 340,2000), HUM MUTAT, 16(2), 2000, pp. 175-175

Authors: Mersiyanova, IV Ismailov, SM Polyakov, AV Dadali, EL Fedotov, VP Nelis, E Lofgren, A Timmerman, V Van Broeckhoven, C Evgrafov, OV

Citation: Iv. Mersiyanova et al., Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32(GJB1) in Russian Charcot-Marie-Tooth neuropathy patients, HUM MUTAT, 15(4), 2000, pp. 340-347

Authors: Mersiyanova, IV Perepelov, AV Polyakov, AV Sitnikov, VF Dadali, EL Oparin, RB Petrin, AN Evgrafov, OV

Citation: Iv. Mersiyanova et al., A new variant of Charcot-Marie-Tooth disease type 2 is probably the resultof a mutation in the neurofilament-light gene, AM J HU GEN, 67(1), 2000, pp. 37-46