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Two case reports of inherited antithrombin deficiency: a novel frameshift mutation and a large deletion including all seven exons detected using two methods

✍ Scribed by Akiko Sekiya; Eriko Morishita; Megumi Karato; Keiko Maruyama; Itsumi Shimogawara; Mika Omote; Yoshiyuki Wakugawa; Moeko Shinohara; Tomoe Hayashi; Yasuko Kadohira; Hidesaku Asakura; Shinji Nakao; Shigeki Ohtake


Book ID
107619209
Publisher
Carden Jennings Publishing
Year
2011
Tongue
English
Weight
233 KB
Volume
93
Category
Article
ISSN
0925-5710

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