Primary familial polycythaemia associated with a novel point mutation in the erythropoietin receptor

British Journal of Haematology

Volumn 99, Issue 1, 1997, Pages 222-227

  Furukawa, Tatsuo ^a,d   Narita, Miwako ^a   Sakaue, Minori ^a   Otsuka, Tomio ^b   Kuroha, Takashi ^a   Masuko, Masayoshi ^a   Azegami, Takuaki ^a   Kishi, Kenji ^a   Takahashi, Masuhiro ^a   Utsumi, Jirou ^c   Koike, Tadashi ^d   Aizawa, Yoshifusa ^a  

^a NIIGATA UNIVERSITY   (Japan)

^b Niigata Prefectural Shibata Hospital   (Japan)

^c Niigata Red Cross Blood Center   (Japan)

^d NIIGATA UNIVERSITY MEDICAL AND DENTAL HOSPITAL   (Japan)

Author keywords

Erythropoietin receptor; PFCP; Point mutation; Polycythaemia; SHP 1

Indexed keywords

ERYTHROPOIETIN RECEPTOR;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CHILD; FAMILIAL DISEASE; FEMALE; HUMAN; POINT MUTATION; POLYCYTHEMIA; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SCHOOL CHILD;

EID: 9844244548     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1997.3583172.x     Document Type: Article

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