Glanzmann thrombasthenia in Pakistan: molecular analysis and identification of novel mutations-Reference-Cited by-同舟云学术

Glanzmann thrombasthenia in Pakistan: molecular analysis and identification of novel mutations

Author:

Haghighi A.¹²,Borhany M.³,Ghazi A.⁴,Edwards N.⁵,Tabaksert A.⁵,Haghighi A.⁶,Fatima N.³,Shamsi T.S.³,Sayer J.A.⁵

Affiliation:

1. Department of GeneticsHarvard Medical School Boston MA USA

2. Department of Medicine and the Howard Hughes Medical InstituteBrigham and Women's Hospital Boston MA USA

3. Department of HematologyHemostasis & Thrombosis of National Institute of Blood Disease & Bone Marrow Transplantation Karachi Pakistan

4. Chronic Pain ClinicWilderman Medicine Professional Corporation Toronto Canada

5. Institute of Genetic MedicineNewcastle University Newcastle UK

6. Toronto General HospitalUniversity of Toronto Toronto Canada

Funder

Wellcome Trust

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference23 articles.

1. Hereditare hamorrhagische thrombasthenie. Ein beitrag zur pathologie der blutplattchen;Glanzmann E;Jb Kinderheilk,1918

5. Glanzmann thrombasthenia: integrin alpha IIb beta 3 deficiency;Tomiyama Y;Int J Hematol,2000

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