000 01386 a2200457 4500
005 20250517033729.0
264 0 _c20160601
008 201606s 0 0 eng d
022 _a1365-2141
024 7 _a10.1111/bjh.13511
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChauveau, Aurélie
245 0 0 _aA new point mutation in EPOR inducing a short deletion in congenital erythrocytosis.
_h[electronic resource]
260 _bBritish journal of haematology
_cFeb 2016
300 _a475-7 p.
_bdigital
500 _aPublication Type: Letter
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aHumans
650 0 4 _aJanus Kinase 2
_xgenetics
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aPoint Mutation
650 0 4 _aPolycythemia
_xcongenital
650 0 4 _aReceptors, Erythropoietin
_xgenetics
650 0 4 _aYoung Adult
700 1 _aLuque Paz, Damien
700 1 _aLecucq, Lydie
700 1 _aLe Gac, Gérald
700 1 _aLe Maréchal, Cédric
700 1 _aGueguen, Paul
700 1 _aBerthou, Christian
700 1 _aUgo, Valérie
773 0 _tBritish journal of haematology
_gvol. 172
_gno. 3
_gp. 475-7
856 4 0 _uhttps://doi.org/10.1111/bjh.13511
_zAvailable from publisher's website
999 _c24934314
_d24934314