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Hereditary Familial Vestibular Degenerative Diseases

✍ Scribed by JOHN C. SUN; ADRIAAN M. van ALPHEN; MARIETTE WAGENAAR; PATRICK HUYGEN; CASPER C. HOOGENRAAD; TAMA HASSON; SEBASTIAAN K. E. KOEKKOEK; BARBARA A. BOHNE; CHRIS I. DE ZEEUW


Book ID
111396992
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
151 KB
Volume
942
Category
Article
ISSN
0890-6564

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## H.S., I.S.) Japan We report a 28-year-old-Japanese male who had a skin tumor derived from variant type xeroderma pigmentosum (XP), combined with factor XI (FXI) deficiency and type llB von Willebrand's disease (vWd). The patient had abnormal bleeding history on tooth extraction. FXI clotting ac