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Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

✍ Scribed by F. Quélin; M. Trossaërt; M. Sigaud; P. D. E. Mazancourt; E. Fressinaud


Book ID
109148271
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
101 KB
Volume
2
Category
Article
ISSN
1538-7933

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