Publication | Closed Access
Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families
154
Citations
0
References
2004
Year
Mendelian DisorderGenetic DisorderInherited Metabolic DiseaseGenetic EpidemiologyNovel MutationsDegenerative DiseaseNeurological PhenotypeNeurologyMedicineItalian FamiliesNeurogenetics
No additional data available for this publication yet. Check back later!