Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease-Reference-Cited by-同舟云学术

Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease

Published:2019-09-18 Issue:6 Volume:25 Page:1035-1044
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Ahmed Shariq¹,Yadegari Hamideh²^ORCID,Naz Arshi¹,Biswas Arijit²,Budde Ulrich³,Saqlain Nazish⁴,Amanat Samina⁵,Tariq Shehla⁴,Raziq Fazle⁶,Masood Shahtaj⁶,Pavlova Anna²,Shamsi Tahir Sultan¹,Oldenburg Johannes²^ORCID

Affiliation:

1. National Institute of Blood Disease & Bone Marrow Transplantation Karachi Pakistan

2. Institute of Experimental Haematology and Transfusion Medicine University Clinics Bonn Bonn Germany

3. Hämostaseology Medilys Laborgesellschaft mbH Hamburg Germany

4. Children Hospital Lahore Lahore Pakistan

5. Atomic Energy Commission Islamabad Islamabad Pakistan

6. Hayatabad Medical Complex Peshawar Peshawar Pakistan

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.13841

Reference33 articles.

1. Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: an international, multicenter study

2. von Willebrand disease

3. Von Willebrand’s Disease

4. Structure of the gene for human von Willebrand factor

5. The genetic basis of von Willebrand disease

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