Publication | Open Access
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
145
Citations
15
References
2013
Year
Mendelian DisorderGenetic DisorderMedicineGeneticsDegenerative DiseaseNeuroscienceMolecular NeurobiologyNeuropathologyBasal GangliaMajor CauseNeurogenetics
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