Transaldolase deficiency caused by the homozygous p.R192C mutation of the TALDO1 gene in four Emirati patients with considerable phenotypic variability
Crossref DOI link: https://doi.org/10.1007/s00431-014-2449-5
Published Online: 2014-11-12
Published Print: 2015-05
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Al-Shamsi, Aisha M.
Ben-Salem, Salma
Hertecant, Jozef
Al-Jasmi, Fatma
Text and Data Mining valid from 2014-11-12