Publication | Closed Access
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification
17
Citations
16
References
2015
Year
New Slc20a2 MutationMendelian DisorderGenetic DisorderGeneticsClinical GeneticsGenetic EpidemiologyNeurologyNeuroscienceNeuropathologyMedicineSouthern Italy FamilyNeurogenetics
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