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Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A gene

✍ Scribed by A. Savoia; Maria Rosaria Piemontese; Maria Savino; Adriana Zatterale; J. Pronk; F. Arwert; Hans Joenje; Ugo Ramenghi; Franca Dagna-Bricarelli; Bruno Dallapiccola; Leopoldo Zelante

Publisher
Springer
Year
1996
Tongue
English
Weight
45 KB
Volume
99
Category
Article
ISSN
0340-6717

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Fanconi anemia (FA) is a rare autosomal recessive or X-linked disorder characterized by aplastic anemia, cancer susceptibility and cellular sensitivity to DNA crosslinking agents. Eight FA proteins (FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL and FANCM) and three non-FA proteins (FAAP100, FAAP24