000 01227 a2200337 4500
005 20250515195511.0
264 0 _c20100401
008 201004s 0 0 eng d
022 _a1521-0669
024 7 _a10.3109/08880010903116413
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDemirel, Nihal
245 0 0 _aSevere purpura fulminans due to coexistence of homozygous protein C deficiency and homozygous methylenetetrahydrofolate reductase mutation.
_h[electronic resource]
260 _bPediatric hematology and oncology
_cNov 2009
300 _a597-600 p.
_bdigital
500 _aPublication Type: Case Reports; Letter
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aMethylenetetrahydrofolate Reductase (NADPH2)
_xgenetics
650 0 4 _aMutation
650 0 4 _aProtein C Deficiency
_xgenetics
650 0 4 _aPurpura Fulminans
_xetiology
700 1 _aBas, Ahmet Yagmur
700 1 _aOkumus, Nurullah
700 1 _aZenciroglu, Ayşegul
700 1 _aYarali, Nese
773 0 _tPediatric hematology and oncology
_gvol. 26
_gno. 8
_gp. 597-600
856 4 0 _uhttps://doi.org/10.3109/08880010903116413
_zAvailable from publisher's website
999 _c19337599
_d19337599