Successful hematopoietic stem cell transplantation in a child with congenital erythropoietic porphyria due to a mutation in GATA‐1

By  

PEDIATRIC TRANSPLANTATION, Vol. 1397-3142, Iss. 7, 2015-11 ,pp. : 803-805

John Wiley & Sons Inc

Access to resources Recommend Favorite

A novel GATA6 mutation associated with congenital ventricular septal defect

By Zheng Gui-Fen   Wei Dong   Zhao Hong   Zhou Ning   Yang Yi-Qing   Liu Xing-Yuan  

International Journal of Molecular Medicine, Vol. 29, Iss. 6, 2012-06 ,pp. : 1065-1071

Spandidos Publications

Access to resources Recommend Favorite

A novel GATA4 mutation responsible for congenital ventricular septal defects

By                    

International Journal of Molecular Medicine, Vol. 28, Iss. 4, 2011-01 ,pp. : 557-564

Spandidos Publications

Access to resources Recommend Favorite

Dyserythropoietic Anemia and Thrombocytopenia due to a Novel Mutation in GATA-1

By  

Acta Haematologica, Vol. 114, Iss. 2, 2005-08 ,pp. : 113-116

Karger

Access to resources Recommend Favorite

The W198X and R173W mutations in the porphobilinogen deaminase gene in acute intermittent porphyria have higher clinical penetrance than R167W. A population-based study

By Andersson C.   Floderus Y.   Wikberg A.   Lithner F.  

Scandinavian Journal of Clinical and Laboratory Investigation, Vol. 60, Iss. 7, 2000-11 ,pp. : 643-648

Informa Healthcare

Access to resources Recommend Favorite