000 01370 a2200421 4500
005 20250513080336.0
264 0 _c19930324
008 199303s 0 0 eng d
022 _a0007-1048
024 7 _a10.1111/j.1365-2141.1993.tb04646.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLorenzo, F
245 0 0 _aSevere poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrin.
_h[electronic resource]
260 _bBritish journal of haematology
_cJan 1993
300 _a152-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aArginine
650 0 4 _aChild, Preschool
650 0 4 _aCysteine
650 0 4 _aErythrocytes, Abnormal
650 0 4 _aGenotype
650 0 4 _aHematologic Diseases
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPolymorphism, Genetic
650 0 4 _aSpectrin
_xgenetics
700 1 _aMiraglia del Giudice, E
700 1 _aAlloisio, N
700 1 _aMorle, L
700 1 _aForissier, A
700 1 _aPerrotta, S
700 1 _aSciarratta, G
700 1 _aIolascon, A
700 1 _aDelaunay, J
773 0 _tBritish journal of haematology
_gvol. 83
_gno. 1
_gp. 152-7
856 4 0 _uhttps://doi.org/10.1111/j.1365-2141.1993.tb04646.x
_zAvailable from publisher's website
999 _c8434593
_d8434593