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Year | Number of Results |
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2003 | 2 |
2015 | 1 |
2016 | 1 |
2019 | 1 |
2024 | 0 |
PubMed (cited) for id: 609552
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Dominant LMAN2L mutation causes intellectual disability with remitting epilepsy.
Ann Clin Transl Neurol. 2019 Mar 7;6(4):807-811. doi: 10.1002/acn3.727. eCollection 2019 Apr.
Ann Clin Transl Neurol. 2019.
PMID: 31020005
Free PMC article.
Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family.
Rafiullah R, Aslamkhan M, Paramasivam N, Thiel C, Mustafa G, Wiemann S, Schlesner M, Wade RC, Rappold GA, Berkel S.
Rafiullah R, et al.
J Med Genet. 2016 Feb;53(2):138-44. doi: 10.1136/jmedgenet-2015-103179. Epub 2015 Nov 13.
J Med Genet. 2016.
PMID: 26566883
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VIPL, a VIP36-like membrane protein with a putative function in the export of glycoproteins from the endoplasmic reticulum.
Neve EP, Svensson K, Fuxe J, Pettersson RF.
Neve EP, et al.
Exp Cell Res. 2003 Aug 1;288(1):70-83. doi: 10.1016/s0014-4827(03)00161-7.
Exp Cell Res. 2003.
PMID: 12878160
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Profile-based data base scanning for animal L-type lectins and characterization of VIPL, a novel VIP36-like endoplasmic reticulum protein.
Nufer O, Mitrovic S, Hauri HP.
Nufer O, et al.
J Biol Chem. 2003 May 2;278(18):15886-96. doi: 10.1074/jbc.M211199200. Epub 2003 Feb 27.
J Biol Chem. 2003.
PMID: 12609988
Free article.
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