Erratum to: ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies
- Resource Type
- Source
- Journal of Inherited Metabolic Disease. 39(5):759-759
- Subject
0301 basic medicine Proximal muscle weakness Ataxia business.industry Anatomy 030105 genetics & heredity medicine.disease Phenotype 03 medical and health sciences Epilepsy Genetics Medicine medicine.symptom business Genetics (clinical) - Language
- English
- ISSN
- 0141-8955