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Journal Abstract Search

640 related items for PubMed ID: 10586262

  • 1. Mutation testing in Charcot-Marie-Tooth neuropathy.
    Nicholson GA.
    Ann N Y Acad Sci; 1999 Sep 14; 883():383-8. PubMed ID: 10586262
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  • 4. Mutation Testing in Charcot-Marie-Tooth Neuropathy.
    Nicholson GA.
    Ann N Y Acad Sci; 1999 Oct 14; 883(1):383-388. PubMed ID: 29086947
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  • 7. [Mutation of the myelin Po gene in hereditary motor and sensory neuropathy].
    Hayasaka K.
    Rinsho Shinkeigaku; 1995 Dec 14; 35(12):1444-6. PubMed ID: 8752425
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  • 9. Molecular analysis in Japanese patients with Charcot-Marie-Tooth disease: DGGE analysis for PMP22, MPZ, and Cx32/GJB1 mutations.
    Numakura C, Lin C, Ikegami T, Guldberg P, Hayasaka K.
    Hum Mutat; 2002 Nov 14; 20(5):392-8. PubMed ID: 12402337
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  • 10. Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot-Marie-Tooth neuropathy patients.
    Choi BO, Lee MS, Shin SH, Hwang JH, Choi KG, Kim WK, Sunwoo IN, Kim NK, Chung KW.
    Hum Mutat; 2004 Aug 14; 24(2):185-6. PubMed ID: 15241803
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  • 11. [PCR in the gene diagnosis of Charcot-Marie-Tooth disease].
    Xiao J, Tang B, Xia J.
    Zhonghua Yi Xue Za Zhi; 2001 Feb 10; 81(3):138-41. PubMed ID: 11798863
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  • 12. [Molecular basis of Charcot-Marie-Tooth neuropathy].
    Hayasaka K.
    Nihon Rinsho; 1996 Aug 10; 54(8):2243-51. PubMed ID: 8810804
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  • 13. Mutations in the peripheral myelin protein zero and connexin32 genes detected by non-isotopic RNase cleavage assay and their phenotypes in Japanese patients with Charcot-Marie-Tooth disease.
    Yoshihara T, Yamamoto M, Doyu M, Mis KI, Hattori N, Hasegawa Y, Mokuno K, Mitsuma T, Sobue G.
    Hum Mutat; 2000 Aug 10; 16(2):177-8. PubMed ID: 10923043
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  • 16. Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B.
    Latour P, Blanquet F, Nelis E, Bonnebouche C, Chapon F, Diraison P, Ollagnon E, Dautigny A, Pham-Dinh D, Chazot G.
    Hum Mutat; 1995 Aug 10; 6(1):50-4. PubMed ID: 7550231
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  • 19. Molecular basis of hereditary neuropathies.
    Chance PF.
    Phys Med Rehabil Clin N Am; 2001 May 10; 12(2):277-91. PubMed ID: 11345007
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