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: Karunas, AS Mersiyanova, IV Polyakov, AV Evgrafov, OV Khusnutdinova, EK

Citation: As. Karunas et al., A study of mutations and haplotypes for polymorphic markers in Wilson-Konovalov disease patients from Bashkortostan, RUSS J GEN, 36(7), 2000, pp. 802-808

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