Author:
Shaikh Shagufta,Shettigar Suresh K. G.,Kumar Santosh,Kantharia Surita,Kurva Jagannath,Cherian Susan
Publisher
Springer Science and Business Media LLC
Reference17 articles.
1. Brogna S. and Wen J. 2009 Nonsense-mediated mRNA decay (NMD) mechanisms. Nat. Struct. Mol. Biol. 16, 107–113.
2. Clayton P. E., Hanson D., Magee L., Murray P. G., Saunders E., Abu-Amero S. N. et al. 2012 Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination. Clin. Endocrinol. (Oxf.) 77, 335–342.
3. Deeb A., Afandi O., Attia S. and El Fatih A. 2015 3-M syndrome: a novel CUL7 mutation associated with respiratory distress and a good response to GH therapy. Endocrinol. Diabetes Metab. Case Rep. 2015, 150012.
4. Hanson D., Murray P. G., Sud A., Temtamy S. A., Aglan M., Superti-Furga A. et al. 2009 The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1. Am. J. Hum. Genet. 84, 801–806.
5. Hanson D., Murray P. G., Black G. C. M. and Clayton P. E. 2011a The genetics of 3-M syndrome: unravelling a potential new regulatory growth pathway. Horm. Res. Paediatr. 76, 369–378.
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