Neu-Laxova syndrome 2

Any Neu-Laxova syndrome in which the cause of the disease is a mutation in the PSAT1 gene.

Also known as: Neu-Laxova syndrome 2, Neu-Laxova syndrome caused by mutation in PSAT1, Neu-Laxova syndrome due to phosphoserine aminotransferase deficiency, Neu-Laxova syndrome type 2, PSAT1 Neu-Laxova syndrome, phosphoserine aminotransferase deficiency, prenatal form, NEU-Laxova syndrome 2, NLS2

0 clinical trials for this condition and its sub-types, 0 tagged with Neu-Laxova syndrome 2 itself.