4 - Bibliothèques de l'Université de Lorraine

134. Lanciotti M. ; Perutelli P. ; Valetta A. ; Di Martino D. ; Murri P.G.
Ankyrine deficiency is the most common defect in dominant
and non dominant hereditary spherocytosis
Haematologica 1997, 82,460-462
135. Yawata Y.
Red cell membrane protein band 4.2 : phenotypic, genetic and
electron microscopic aspects
Biochimica and Biophysica Acta 1994, 131-148
136. Kanzaki A. ; Yasunaga M. ; Okamoto N. ; Inoue T. ; Yawata A. ;
Wada H. ; Andoh A. ; Hodohara K. ; Fu jiyama Y. ; Bamba T. ;
Harano T. ; Harano K. ; Yawata Y.
Band 4.2 5higa : 317 CGC @ TGC in compound heterozygot
with 142 GCT @ ACT results in band 4.2 deficiency an
microspherocytosis
Br Haematol1995, 91,333-340
137. Kanzaki A. ; Yawata Y. ; Yawata A. ; Inoue T. ; Okamoto N. ;
Wada H. ; Harano T. ; Harano K. ; Wi Imotte R. ; Hayette S. ;
Nakamura Y. ; Niki J. ; Kawamura Y. ; Nakamura S. ; Matsuda M.
Band 4.2 Kamatsu 526 GAT @ TAT (175 Asp @ Tyr) in exon 4
of the band 4.2 gene associated with total deficiency of band
4.2, hemolytic anemia with ovalo-stomatocytosis and masked
disruption of the cytosqueletal network
Int J Hematol1995, 61, 165-178
138. Hayette S. ; Morle L. ; Bozon M. ; Ghaner A. ; Risinger M. ;
Korsgren C. ; Tanner M.J. ; Fattoum S. ; Cohen C.M. ; Delaunay J.
A point mutation in the protein 4.2 gene (allele 4.2 Tozeur)
associated with hereditary hemolytic anemia
Br J Haematol1995, 89, 762-770