Severe congenital hemolytic anemia caused by a novel compound heterozygous PKLR gene mutation in a Chinese boy

[1] Primary red cell hydration disorders: Pathogenesis and diagnosis.[J].A. Caulier;R. Rapetti‐Mauss;H. Guizouarn;V. Picard;L. Gar?on;C. Badens.International Journal of Laboratory Hematology.2018,

[2] A Novel and a Previously Described Compound Heterozygous PKLR Gene Mutations Causing Pyruvate Kinase Deficiency in a Chinese Child [J]. FETAL AND PEDIATRIC PATHOLOGY, 2014, 33 (03) : 182 - 190

[3] A novel mutation causing pyruvate kinase deficiency responsible for a severe neonatal respiratory distress syndrome and jaundice [J]. EUROPEAN JOURNAL OF PEDIATRICS, 2001, 160 (08) : 523 - 524

[1] Primary red cell hydration disorders: Pathogenesis and diagnosis.[J].A. Caulier;R. Rapetti‐Mauss;H. Guizouarn;V. Picard;L. Gar?on;C. Badens.International Journal of Laboratory Hematology.2018,

[2] A Novel and a Previously Described Compound Heterozygous PKLR Gene Mutations Causing Pyruvate Kinase Deficiency in a Chinese Child [J]. FETAL AND PEDIATRIC PATHOLOGY, 2014, 33 (03) : 182 - 190

[3] A novel mutation causing pyruvate kinase deficiency responsible for a severe neonatal respiratory distress syndrome and jaundice [J]. EUROPEAN JOURNAL OF PEDIATRICS, 2001, 160 (08) : 523 - 524