Neonatal hemolytic anemia due to inherited harderoporphyria: Clinical characteristics and molecular basis

Blood

Volumn 91, Issue 4, 1998, Pages 1453-1457

  Lamoril, J ^b   Puy, H ^b   Gouya, L ^b   Rosipal, R ^b   Da Silva, V ^b   Grandchamp, B ^b   Foint, T ^b   Bader Meunier, B ^b   Dommergues, J P ^b   Deybach, J C ^b   Nordmann, Y ^a  

^a HÔPITAL LOUIS MOURIER   (France)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

COPROPORPHYRINOGEN;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CONTROLLED STUDY; ERYTHROPOIESIS; EXON; GENE MUTATION; HARDEROPORPHYRIA; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; NEWBORN; NEWBORN HEMOLYTIC DISEASE; PHOTOSENSITIVITY DISORDER; PORPHYRIA; PRIORITY JOURNAL;

EID: 0032519497     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v91.4.1453     Document Type: Article

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