Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to gamma-glutamylcysteine synthetase deficiency in a patient of Moroccan origin.

Haematologica

Volumn 92, Issue 11, 2007, Pages

  Manu Pereira M ^a   Gelbart, T ^b   Ristoff, E ^b   Crain, K C ^b   Bergua, J M ^b   Lopez Lafuente A ^b   Kalko, S G ^b   Garcia Mateos E ^b   Beutler, E ^b   Vives Corrons, J L ^b  

^a UNIVERSITY OF BARCELONA   (Spain)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

GLUTAMATE CYSTEINE LIGASE;

ARTICLE; CASE REPORT; ENZYMOLOGY; FAMILY HEALTH; GENETICS; HEREDITARY HEMOLYTIC ANEMIA; HOMOZYGOTE; HUMAN; MALE; MOROCCO; NEUROLOGIC DISEASE; POINT MUTATION; PRESCHOOL CHILD;

ANEMIA, HEMOLYTIC, CONGENITAL NONSPHEROCYTIC; CHILD, PRESCHOOL; FAMILY HEALTH; GLUTAMATE-CYSTEINE LIGASE; HOMOZYGOTE; HUMANS; MALE; MOROCCO; NERVOUS SYSTEM DISEASES; POINT MUTATION;

MLCS; MLOWN;

EID: 65049084484     PISSN: None     EISSN: 15928721     Source Type: Journal    
DOI: 10.3324/haematol.11238     Document Type: Article

References (0)