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PubMed (cited) for id: 613114
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Mutation in FAM134B causing hereditary sensory neuropathy with spasticity in a Turkish family.
Muscle Nerve. 2014 May;49(5):774-5. doi: 10.1002/mus.24145.
Muscle Nerve. 2014.
PMID: 24327336
No abstract available.
Regulation of endoplasmic reticulum turnover by selective autophagy.
Khaminets A, Heinrich T, Mari M, Grumati P, Huebner AK, Akutsu M, Liebmann L, Stolz A, Nietzsche S, Koch N, Mauthe M, Katona I, Qualmann B, Weis J, Reggiori F, Kurth I, Hübner CA, Dikic I.
Khaminets A, et al.
Nature. 2015 Jun 18;522(7556):354-8. doi: 10.1038/nature14498. Epub 2015 Jun 3.
Nature. 2015.
PMID: 26040720
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Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy.
Kurth I, Pamminger T, Hennings JC, Soehendra D, Huebner AK, Rotthier A, Baets J, Senderek J, Topaloglu H, Farrell SA, Nürnberg G, Nürnberg P, De Jonghe P, Gal A, Kaether C, Timmerman V, Hübner CA.
Kurth I, et al.
Nat Genet. 2009 Nov;41(11):1179-81. doi: 10.1038/ng.464. Epub 2009 Oct 18.
Nat Genet. 2009.
PMID: 19838196
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Oncogenic properties of a novel gene JK-1 located in chromosome 5p and its overexpression in human esophageal squamous cell carcinoma.
Tang WK, Chui CH, Fatima S, Kok SH, Pak KC, Ou TM, Hui KS, Wong MM, Wong J, Law S, Tsao SW, Lam KY, Beh PS, Srivastava G, Chan AS, Ho KP, Tang JC.
Tang WK, et al.
Int J Mol Med. 2007 Jun;19(6):915-23.
Int J Mol Med. 2007.
PMID: 17487424
Free article.
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