1.
Rev Neurol
; 59(8): 382-3, 2014 Oct 16.
Article
in Spanish
| MEDLINE
| ID: mdl-25297483
Subject(s)
AMP Deaminase/deficiency , Purine-Pyrimidine Metabolism, Inborn Errors/genetics , AMP Deaminase/genetics , Amino Acid Substitution , Child , Female , Homozygote , Humans , Mutation, Missense , Physical Examination , Point Mutation , Protein Isoforms/deficiency , Protein Isoforms/genetics , Purine-Pyrimidine Metabolism, Inborn Errors/diagnosis
2.
Rev. neurol. (Ed. impr.)
; 59(8): 382-383, 16 oct., 2014.
Article
in Spanish
| IBECS
| ID: ibc-128126
ABSTRACT
No disponible