4 - Bibliothèques de l'Université de Lorraine

96. Delaunay J. ; Dhermy D.
Le squelette érythrocytaire et les maladies génétiques de la
forme du globule rouge
Med Sci 1990,6,562-570
97. Peters L. ; Lux S.E.
Ankyrins : structure and function in normal cells and
hereditary spherocytosis
Sem in Haematol Vol 30 N°2, April 1993, 85-118
98. Davies C.H. ; Bennet B.
Mapping in binding site of human erythrocyt ankyrine for the
anion exchanges and spectrin
J Biol Chem 1990, 265,10589-10596
99. Hassoun H. ; Vassiliadis J.N. ; Murray J. ; NJolstad P.R. ; Rogus
J.J. ; Ballas S.K. ; Schaeffer G. ; Jarolim P. ; Brabek V. ; PalekJ.
Characterization of the underlying molecular defect in
hereditary spherocytosis associated with spectrin deficiency
Blood Vol 90 N°l, July 1997, 398-406
100. Palek J. ; Jarolim P.
Clinical expression and laboratory detection of red blud cellu
membrane protein mutations
Seminar haematology Vol 30 N°4, October 1993, 249-283
101. Agre P. ; Castella J.F. ; Zinkham W.H. ; Mc Millan C. ; Bennet V.
Partial deficienty of erythrocyte spectrin in hereditary
spherocytosis
Nature 1985,314,380-383
102. Costa F.F. ; Agre P. ; Watkins P.C. ; Winkelmann J.C. ; Tang T.K. ;
John K.M. ; Lux S.E. ; Forget B.G.
Linkage of dominante hereditary spherocytosis to the gene for
the erythrocyte membrane skeleton protein ankyrin
N Engl S Med 1990,323,1046-1050