Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Akber Najmuddin"'
Autor:
Arshi Naz, Muhammad Younus Jamal, Samina Amanat, Ikram Din ujjan, Akber Najmuddin, Humayun Patel, Fazle Raziq, Nisar Ahmed, Ayisha Imran, Tahir Sultan Shamsi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-7 (2017)
Abstract Background Autosomal recessive bleeding disorders (ARBDs) include deficiencies of clotting factors I, II, V, VII, X, XI, XIII, vitamin K dependent clotting factors, combined factor V & VIII, Von Willebrand Disease (vWD) type 3, Glanzmann’s
Externí odkaz:
https://doaj.org/article/d98164047c44450b892d10d2d7f3382d
Autor:
Ayisha Imran, Akber Najmuddin, Arshi Naz, Muhammad Younus Jamal, Samina Tufail Amanat, Nisar Ahmed, Fazle Raziq, Ikram Din Ujjan, Tahir Shamsi, Humayun Patel
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-7 (2017)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Autosomal recessive bleeding disorders (ARBDs) include deficiencies of clotting factors I, II, V, VII, X, XI, XIII, vitamin K dependent clotting factors, combined factor V & VIII, Von Willebrand Disease (vWD) type 3, Glanzmann’s thrombas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d7fab41a7e70323bff115bc2b8f9fa9