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Imerslund-Gräsbeck syndrome: new mutation in amnionless.
Densupsoontorn N, Sanpakit K, Vijarnsorn C, Pattaragarn A, Kangwanpornsiri C, Jatutipsompol C, Tirapongporn H, Jirapinyo P, Shah NP, Sturm AC, Tanner SM. Densupsoontorn N, et al. Among authors: sturm ac. Pediatr Int. 2012 Jun;54(3):e19-21. doi: 10.1111/j.1442-200X.2011.03482.x. Pediatr Int. 2012. PMID: 22631584 No abstract available.
Familial peripheral keratopathy without PAX6 mutation.
Smith WM, Lange JM, Sturm AC, Tanner SM, Mauger TF. Smith WM, et al. Among authors: sturm ac. Cornea. 2012 Feb;31(2):130-3. doi: 10.1097/ICO.0b013e3182222779. Cornea. 2012. PMID: 22146551
Hereditary intrinsic factor deficiency in chaldeans.
Sturm AC, Baack EC, Armstrong MB, Schiff D, Zia A, Savasan S, de la Chapelle A, Tanner SM. Sturm AC, et al. JIMD Rep. 2013;7:13-8. doi: 10.1007/8904_2012_133. Epub 2012 Mar 18. JIMD Rep. 2013. PMID: 23430489 Free PMC article.
150 results