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Year | Number of Results |
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2001 | 1 |
2012 | 1 |
2013 | 1 |
2014 | 1 |
2024 | 0 |
PubMed (cited) for id: 615292
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A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2.
J Bone Miner Res. 2014 Apr;29(4):992-8. doi: 10.1002/jbmr.2091.
J Bone Miner Res. 2014.
PMID: 23996431
Free article.
FAM111A mutations result in hypoparathyroidism and impaired skeletal development.
Unger S, Górna MW, Le Béchec A, Do Vale-Pereira S, Bedeschi MF, Geiberger S, Grigelioniene G, Horemuzova E, Lalatta F, Lausch E, Magnani C, Nampoothiri S, Nishimura G, Petrella D, Rojas-Ringeling F, Utsunomiya A, Zabel B, Pradervand S, Harshman K, Campos-Xavier B, Bonafé L, Superti-Furga G, Stevenson B, Superti-Furga A.
Unger S, et al.
Am J Hum Genet. 2013 Jun 6;92(6):990-5. doi: 10.1016/j.ajhg.2013.04.020. Epub 2013 May 16.
Am J Hum Genet. 2013.
PMID: 23684011
Free PMC article.
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Identification of FAM111A as an SV40 host range restriction and adenovirus helper factor.
Fine DA, Rozenblatt-Rosen O, Padi M, Korkhin A, James RL, Adelmant G, Yoon R, Guo L, Berrios C, Zhang Y, Calderwood MA, Velmurgan S, Cheng J, Marto JA, Hill DE, Cusick ME, Vidal M, Florens L, Washburn MP, Litovchick L, DeCaprio JA.
Fine DA, et al.
PLoS Pathog. 2012;8(10):e1002949. doi: 10.1371/journal.ppat.1002949. Epub 2012 Oct 18.
PLoS Pathog. 2012.
PMID: 23093934
Free PMC article.
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Prediction of the coding sequences of unidentified human genes. XXI. The complete sequences of 60 new cDNA clones from brain which code for large proteins.
Nagase T, Kikuno R, Ohara O.
Nagase T, et al.
DNA Res. 2001 Aug 31;8(4):179-87. doi: 10.1093/dnares/8.4.179.
DNA Res. 2001.
PMID: 11572484
Free article.
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