Article metrics
Other content recommended for you
- P19 Clinical pearl: pharmaceutical management of siblings with guanidinoacetate methyltransferase (gamt) deficiency
- Phenotype and genotype in 101 males with X-linked creatine transporter deficiency
- GP223 Creatine deficiency disorders the all-ireland experience
- Neurodegenerative disorders and metabolic disease
- Investigating adults with early-onset epilepsy and intellectual or physical disability
- POE05 A low creatinine in developmental delay, epilepsy and movement disorders—does it matter?
- Creatine transporter deficiency, an underdiagnosed cause of male intellectual disability
- 4CPS-188 Galenic preparations and rare diseases: guanidinoacetate methyltransferase deficiency: experience in a local hospital
- PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease
- Highlights from this issue