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Year | Number of Results |
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1996 | 1 |
1998 | 1 |
2020 | 1 |
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PubMed (OMIM) for id: 8729
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De Novo and Inherited Variants in GBF1 are Associated with Axonal Neuropathy Caused by Golgi Fragmentation.
Am J Hum Genet. 2020 Oct 1;107(4):763-777. doi: 10.1016/j.ajhg.2020.08.018. Epub 2020 Sep 15.
Am J Hum Genet. 2020.
PMID: 32937143
Free PMC article.
Human GBF1 is a ubiquitously expressed gene of the sec7 domain family mapping to 10q24.
Mansour SJ, Herbrick JA, Scherer SW, Melançon P.
Mansour SJ, et al.
Genomics. 1998 Dec 1;54(2):323-7. doi: 10.1006/geno.1998.5563.
Genomics. 1998.
PMID: 9828135
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Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain.
Nagase T, Seki N, Ishikawa K, Ohira M, Kawarabayasi Y, Ohara O, Tanaka A, Kotani H, Miyajima N, Nomura N.
Nagase T, et al.
DNA Res. 1996 Oct 31;3(5):321-9, 341-54. doi: 10.1093/dnares/3.5.321.
DNA Res. 1996.
PMID: 9039502
Free article.
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