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Journal Abstract Search

408 related items for PubMed ID: 19651702

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  • 3. Molecular genetics of hereditary sensory neuropathies.
    Auer-Grumbach M, Mauko B, Auer-Grumbach P, Pieber TR.
    Neuromolecular Med; 2006; 8(1-2):147-58. PubMed ID: 16775373
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  • 4. SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies.
    Klein CJ, Wu Y, Kruckeberg KE, Hebbring SJ, Anderson SA, Cunningham JM, Dyck PJ, Klein DM, Thibodeau SN, Dyck PJ.
    J Neurol Neurosurg Psychiatry; 2005 Jul; 76(7):1022-4. PubMed ID: 15965219
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  • 9. Expression pattern analysis and characterization of the hereditary sensory and autonomic neuropathy 2 A (HSAN2A) gene with no lysine kinase (WNK1) in human dorsal root ganglion.
    Sapio MR, King DM, Staedtler ES, Maric D, Jahanipour J, Kurochkina NA, Manalo AP, Ghetti A, Mannes AJ, Iadarola MJ.
    Exp Neurol; 2023 Dec; 370():114552. PubMed ID: 37793538
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  • 10. Novel mutation in the HSN2 gene in a Korean patient with hereditary sensory and autonomic neuropathy type 2.
    Cho HJ, Kim BJ, Suh YL, An JY, Ki CS.
    J Hum Genet; 2006 Dec; 51(10):905-908. PubMed ID: 16946995
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  • 11. The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA.
    Wang JJ, Yu B, Li Z.
    BMC Med Genet; 2019 May 27; 20(1):91. PubMed ID: 31132985
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  • 12. Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutation.
    Suh BC, Hong YB, Nakhro K, Nam SH, Chung KW, Choi BO.
    Mol Med Rep; 2014 Feb 27; 9(2):481-6. PubMed ID: 24247255
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  • 14. A novel RAB7 mutation associated with ulcero-mutilating neuropathy.
    Houlden H, King RH, Muddle JR, Warner TT, Reilly MM, Orrell RW, Ginsberg L.
    Ann Neurol; 2004 Oct 27; 56(4):586-90. PubMed ID: 15455439
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  • 15. A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV).
    Shaikh SS, Chen YC, Halsall SA, Nahorski MS, Omoto K, Young GT, Phelan A, Woods CG.
    Hum Mutat; 2017 Jan 27; 38(1):55-63. PubMed ID: 27676246
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  • 19. A novel homozygous mutation in the WNK1/HSN2 gene causing hereditary sensory neuropathy type 2.
    Potulska-Chromik A, Kabzińska D, Lipowska M, Kostera-Pruszczyk A, Kochański A.
    Acta Biochim Pol; 2012 Jan 27; 59(3):413-5. PubMed ID: 22910560
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  • 20. Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.
    Indo Y.
    Clin Auton Res; 2002 May 27; 12 Suppl 1():I20-32. PubMed ID: 12102460
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