Autosomal recessive inherited bleeding disorders in Pakistan: a cross-sectional study from selected regions

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 thrombasthenia (GT) and Bernard–Soulier syndrome. Patie...

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Bibliografiska uppgifter
I publikationen:Orphanet J Rare Dis
Huvudupphovsmän: Naz, Arshi, Jamal, Muhammad Younus, Amanat, Samina, Din ujjan, Ikram, Najmuddin, Akber, Patel, Humayun, Raziq, Fazle, Ahmed, Nisar, Imran, Ayisha, Shamsi, Tahir Sultan
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2017
Ämnen:
Research
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5383974/
https://ncbi.nlm.nih.gov/pubmed/28388959
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-017-0620-6
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