Author:
Zafarghandi Motlagh F.,Fallah M. S.,Bagherian H.,Shirzadeh T.,Ghasri S.,Dabbagh S.,Jamali M.,Salehi Z.,Abiri M.,Zeinali S.
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics (clinical),General Medicine
Reference17 articles.
1. Poon MC, D’Oiron R, Von Depka M, Khair K, Negrier C, Karafoulidou A, Huth-Kuehne A, Morfini M. International data collection on recombinant factor V, congenital platelet disorders study G: prophylactic and therapeutic recombinant factor VIIa administration to patients with Glanzmann's thrombasthenia: results of an international survey. J Thromb Haemost. 2004;2:1096–103.
2. Handin RI. Inherited platelet disorders. Hematology Am Soc Hematol Educ Program. 2005;1:396–402.
3. Pillitteri D, Pilgrimm AK, Kirchmaier CM. Novel mutations in the GPIIb and GPIIIa genes in Glanzmann Thrombasthenia. Transfus Med Hemother. 2010;37(5):268–77.
4. Rosenberg N, Hauschner H, Peretz H, Mor-Cohen R, Landau M, Shenkman B, Kenet G, Coller BS, Awidi AA, Seligsohn U. A 13-bp deletion in alpha (IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia. J Thromb Haemost. 2005;3:2764–72.
5. Wilcox DA, Wautier JL, Pidard D, Newman PJ. A single amino acid substitution flanking the fourth calcium binding domain of alpha IIb prevents maturation of the alpha IIb beta 3 integrin complex. J Biol Chem. 1994;269:4450–7.
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