PubMed (OMIM) for id: 350076

Year	Number of Results
1986	1
1992	1
1993	1
1994	1
1996	1
1997	1
2001	2
2004	1
2024	0

1

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.

Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, Rochelle J, Dadali EL, Zappia M, Nelis E, Patitucci A, Senderek J, Parman Y, Evgrafov O, Jonghe PD, Takahashi Y, Tsuji S, Pericak-Vance MA, Quattrone A, Battaloglu E, Polyakov AV, Timmerman V, Schröder JM, Vance JM. Züchner S, et al. Nat Genet. 2004 May;36(5):449-51. doi: 10.1038/ng1341. Epub 2004 Apr 4. Nat Genet. 2004. PMID: 15064763 No abstract available.

2

Genomic structure and mutational analysis of the human KIF1B gene which is homozygously deleted in neuroblastoma at chromosome 1p36.2.

Yang HW, Chen YZ, Takita J, Soeda E, Piao HY, Hayashi Y. Yang HW, et al. Oncogene. 2001 Aug 16;20(36):5075-83. doi: 10.1038/sj.onc.1204456. Oncogene. 2001. PMID: 11526494

3

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.

4

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

5

The novel gene D4Mil1e maps to mouse chromosome 4 and human chromosome 1p36.

Gong TL, Burmeister M, Lomax MI. Gong TL, et al. Mamm Genome. 1996 Oct;7(10):790-1. doi: 10.1007/s003359900237. Mamm Genome. 1996. PMID: 8854876 No abstract available.

6

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

7

KIF1B, a novel microtubule plus end-directed monomeric motor protein for transport of mitochondria.

Nangaku M, Sato-Yoshitake R, Okada Y, Noda Y, Takemura R, Yamazaki H, Hirokawa N. Nangaku M, et al. Cell. 1994 Dec 30;79(7):1209-20. doi: 10.1016/0092-8674(94)90012-4. Cell. 1994. PMID: 7528108

8

Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family.

Berciano J, Combarros O, Figols J, Calleja J, Cabello A, Silos I, Coria F. Berciano J, et al. Brain. 1986 Oct;109 ( Pt 5):897-914. doi: 10.1093/brain/109.5.897. Brain. 1986. PMID: 3022865

9

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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