TY  - GEN
AU  - Demirel,Nihal
AU  - Bas,Ahmet Yagmur
AU  - Okumus,Nurullah
AU  - Zenciroglu,Ayşegul
AU  - Yarali,Nese
TI  - Severe purpura fulminans due to coexistence of homozygous protein C deficiency and homozygous methylenetetrahydrofolate reductase mutation
SN  - 1521-0669
PY  - 2010///0401
KW  - Homozygote
KW  - Humans
KW  - Infant, Newborn
KW  - Male
KW  - Methylenetetrahydrofolate Reductase (NADPH2)
KW  - genetics
KW  - Mutation
KW  - Protein C Deficiency
KW  - Purpura Fulminans
KW  - etiology
N1  - Publication Type: Case Reports; Letter
UR  - https://doi.org/10.3109/08880010903116413
ER  -