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Year | Number of Results |
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2001 | 1 |
2017 | 1 |
2020 | 1 |
2025 | 0 |
PubMed (cited) for id: 617612
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Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome.
J Clin Invest. 2020 Aug 3;130(8):4423-4439. doi: 10.1172/JCI131656.
J Clin Invest. 2020.
PMID: 32453716
Free PMC article.
Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Nagase T, Nakayama M, Nakajima D, Kikuno R, Ohara O.
Nagase T, et al.
DNA Res. 2001 Apr 27;8(2):85-95. doi: 10.1093/dnares/8.2.85.
DNA Res. 2001.
PMID: 11347906
Free article.
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Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.
Van De Weghe JC, Rusterholz TDS, Latour B, Grout ME, Aldinger KA, Shaheen R, Dempsey JC, Maddirevula S, Cheng YH, Phelps IG, Gesemann M, Goel H, Birk OS, Alanzi T, Rawashdeh R, Khan AO; University of Washington Center for Mendelian Genomics; Bamshad MJ, Nickerson DA, Neuhauss SCF, Dobyns WB, Alkuraya FS, Roepman R, Bachmann-Gagescu R, Doherty D.
Van De Weghe JC, et al.
Am J Hum Genet. 2017 Jul 6;101(1):23-36. doi: 10.1016/j.ajhg.2017.05.010. Epub 2017 Jun 15.
Am J Hum Genet. 2017.
PMID: 28625504
Free PMC article.
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