Factor X Deficiency with Heterozygous Mutations of Novel p.G435S and Known p.G244R in a Patient Presenting with Severe Umbilical Hemorrhage-Reference-Cited by-同舟云学术

Factor X Deficiency with Heterozygous Mutations of Novel p.G435S and Known p.G244R in a Patient Presenting with Severe Umbilical Hemorrhage

Published:2016 Issue:1.2 Volume:63 Page:23-28
ISSN:0023-5679
Container-title:The Kurume Medical Journal
language:en
Short-container-title:Kurume Med. J.

Author:

MATSUO YOKO¹,MIZUOCHI TATSUKI¹,MIHO MITSUO¹,NAKAGAWA SHINICHIRO¹,OZONO SHUICHI¹,UEDA KOICHIRO¹,SOGABE YOKO²,SEKI RITSUKO²,SOEJIMA KENJI³,OKAMURA TAKASHI²⁴,YAMASHITA YUSHIRO¹

Affiliation:

1. Department of Pediatrics and Child Health, Kurume University School of Medicine

2. Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine

3. R&D Department, The Chemo-Sero-Therapeutic Research Institute

4. Hematology and Oncology Center, St. Mary’s Hospital

Publisher

Kurume Medical Journal

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/kurumemedj/63/1.2/63_MS6300007/_pdf

Reference17 articles.

1. 1. Menegatti M and Peyvandi F. Factor X deficiency. Semin Thromb Hemost. 2009 Jun; 35:407-415.

2. 2. Tuddenham EGD and Cooper DN. The molecular genetics of haemostasis and its inherited disorders. Oxford Monographs on Medical Genetics No.25. Oxford University Press (New York) 1994: p. 122-133.

3. 3. Leytus SP, Foster DC, Kurachi K, and Davie EW. Gene for human factor X: A blood coagulation factor whose gene organization is essentially identical with that of factor IX and protein C. Biochemistry 1986; 25:5098-5102.

4. 4. Royle NJ, Fung MR, MacGillivary RT, and Hamerton JL. The gene for clotting factor 10 is mapped to 13q32→qter. Cytogen Cell Gent. 1986; 41:185-188.

5. 5. Brown DL and Kouides PA. Diagnosis and treatment of inherited factor X deficiency. Haemophilia 2008; 14:1176-1182.

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