Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population-Reference-Cited by-同舟云学术

Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population

Published:2021-08-30 Issue:6 Volume:27 Page:1022-1027
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Shen Ming‐Ching¹²³^ORCID,Wang Jiaan‐Der⁴⁵⁶^ORCID,Tsai Woei²,Lin Ching‐Yeh¹,Lin Jen‐Shiou⁷,Kuo Su‐Feng⁷,Lin Po‐Te¹,Huang Ying‐Chih¹,Hung Mei‐Hua³

Affiliation:

1. Department of Internal Medicine Changhua Christian Hospital Changhua Taiwan

2. Department of Internal Medicine National Taiwan University Hospital Taipei Taiwan

3. Department of Laboratory Medicine National Taiwan University Hospital Taipei Taiwan

4. Center for Rare Disease and Haemophilia Taichung Veterans General Hospital Taichung Taiwan

5. Department of Industrial Engineering and Enterprise Information Tunghai University Taichung Taiwan

6. National Chung Hsing University Taichung Taiwan

7. Department of Laboratory Medicine Changhua Christian Hospital Changhua Taiwan

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.14399

Reference30 articles.

1. Rare bleeding disorders: diagnosis and treatment

2. Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders

3. Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH

4. Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia;Neerman‐Arbez M;Blood,2000

5. Thromboembolism in patients with congenital afibrinogenaemia

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