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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1994 | 1 |
2005 | 1 |
2009 | 1 |
2010 | 2 |
2011 | 1 |
2024 | 0 |
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Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C.
Nat Genet. 2010 Feb;42(2):160-4. doi: 10.1038/ng.508. Epub 2009 Dec 27.
Nat Genet. 2010.
PMID: 20037588
Free PMC article.
Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23-q24.
McEntagart ME, Reid SL, Irrthum A, Douglas JB, Eyre KE, Donaghy MJ, Anderson NE, Rahman N.
McEntagart ME, et al.
Ann Neurol. 2005 Feb;57(2):293-7. doi: 10.1002/ana.20375.
Ann Neurol. 2005.
PMID: 15668982
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CMT2C with vocal cord paresis associated with short stature and mutations in the TRPV4 gene.
Chen DH, Sul Y, Weiss M, Hillel A, Lipe H, Wolff J, Matsushita M, Raskind W, Bird T.
Chen DH, et al.
Neurology. 2010 Nov 30;75(22):1968-75. doi: 10.1212/WNL.0b013e3181ffe4bb.
Neurology. 2010.
PMID: 21115951
Free PMC article.
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Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis.
Dyck PJ, Litchy WJ, Minnerath S, Bird TD, Chance PF, Schaid DJ, Aronson AE.
Dyck PJ, et al.
Ann Neurol. 1994 May;35(5):608-15. doi: 10.1002/ana.410350515.
Ann Neurol. 1994.
PMID: 8179305
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Striking phenotypic variability in familial TRPV4-axonal neuropathy spectrum disorder.
Aharoni S, Harlalka G, Offiah A, Shuper A, Crosby AH, McEntagart M.
Aharoni S, et al.
Am J Med Genet A. 2011 Dec;155A(12):3153-6. doi: 10.1002/ajmg.a.34327. Epub 2011 Nov 7.
Am J Med Genet A. 2011.
PMID: 22065612
No abstract available.
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