Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
W Eyaid, T Al Harbi, S Anazi… - Journal of Inherited …, 2013 - Wiley Online Library
Purpose Transaldolase deficiency is a recently described inborn error of pentose phosphate
pathway. We conducted this study to further delineate the associated phenotype. Methods …
pathway. We conducted this study to further delineate the associated phenotype. Methods …
Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype.
W Eyaid, T Al Harbi, S Anazi, MM Wamelink… - Journal of Inherited …, 2013 - europepmc.org
Purpose Transaldolase deficiency is a recently described inborn error of pentose phosphate
pathway. We conducted this study to further delineate the associated phenotype. Methods …
pathway. We conducted this study to further delineate the associated phenotype. Methods …
Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
W Eyaid, T Al Harbi, S Anazi… - Journal of inherited …, 2013 - pubmed.ncbi.nlm.nih.gov
Purpose Transaldolase deficiency is a recently described inborn error of pentose phosphate
pathway. We conducted this study to further delineate the associated phenotype. Methods …
pathway. We conducted this study to further delineate the associated phenotype. Methods …
Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
W Eyaid, T Al Harbi, S Anazi, MMC Wamelink… - Journal of Inherited …, 2013 - Springer
Purpose Transaldolase deficiency is a recently described inborn error of pentose phosphate
pathway. We conducted this study to further delineate the associated phenotype. Methods …
pathway. We conducted this study to further delineate the associated phenotype. Methods …
Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
W Eyaid, T Al Harbi, S Anazi, MMC Wamelink… - Journal of Inherited …, 2013 - infona.pl
Purpose Transaldolase deficiency is a recently described inborn error of pentose phosphate
pathway. We conducted this study to further delineate the associated phenotype. Methods …
pathway. We conducted this study to further delineate the associated phenotype. Methods …
[PDF][PDF] Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
W Eyaid, T Al Harbi, S Anazi, MMC Wamelink… - 2013 - academia.edu
Purpose Transaldolase deficiency is a recently described inborn error of pentose phosphate
pathway. We conducted this study to further delineate the associated phenotype. Methods …
pathway. We conducted this study to further delineate the associated phenotype. Methods …
[引用][C] Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
W EYAID, T AL HARBI, S ANAZI… - Journal of inherited …, 2013 - pascal-francis.inist.fr
Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple …
CNRS Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple …
Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
W Eyaid, T Al Harbi, S Anazi, M Mirjam… - Journal of Inherited …, 2013 - search.proquest.com
Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
Page 1 ORIGINAL ARTICLE Transaldolase deficiency: report of 12 new cases and further …
Page 1 ORIGINAL ARTICLE Transaldolase deficiency: report of 12 new cases and further …
[引用][C] Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
W Eyaid, T Al Harbi, S Anazi… - Journal of …, 2013 - researchinformation.amsterdamumc …
Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype —
Amsterdam UMC research portal Skip to main navigation Skip to search Skip to main content …
Amsterdam UMC research portal Skip to main navigation Skip to search Skip to main content …
[引用][C] Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype
W Eyaid, T Al Harbi, S Anazi, MMC Wamelink… - Journal of Inherited …, 2013 - cir.nii.ac.jp