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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 1 |
1993 | 1 |
1997 | 1 |
2001 | 1 |
2018 | 1 |
2024 | 0 |
PubMed (cited) for id: 118210
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KIF1Bβ mutations detected in hereditary neuropathy impair IGF1R transport and axon growth.
J Cell Biol. 2018 Oct 1;217(10):3480-3496. doi: 10.1083/jcb.201801085. Epub 2018 Aug 20.
J Cell Biol. 2018.
PMID: 30126838
Free PMC article.
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta.
Zhao C, Takita J, Tanaka Y, Setou M, Nakagawa T, Takeda S, Yang HW, Terada S, Nakata T, Takei Y, Saito M, Tsuji S, Hayashi Y, Hirokawa N.
Zhao C, et al.
Cell. 2001 Jun 1;105(5):587-97. doi: 10.1016/s0092-8674(01)00363-4.
Cell. 2001.
PMID: 11389829
Free article.
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Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A.
Saito M, Hayashi Y, Suzuki T, Tanaka H, Hozumi I, Tsuji S.
Saito M, et al.
Neurology. 1997 Dec;49(6):1630-5. doi: 10.1212/wnl.49.6.1630.
Neurology. 1997.
PMID: 9409358
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Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.
Ben Othmane K, Middleton LT, Loprest LJ, Wilkinson KM, Lennon F, Rozear MP, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA, et al.
Ben Othmane K, et al.
Genomics. 1993 Aug;17(2):370-5. doi: 10.1006/geno.1993.1334.
Genomics. 1993.
PMID: 8406488
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Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease.
Hentati A, Lamy C, Melki J, Zuber M, Munnich A, de Recondo J.
Hentati A, et al.
Genomics. 1992 Jan;12(1):155-7. doi: 10.1016/0888-7543(92)90419-s.
Genomics. 1992.
PMID: 1733853
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