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Case Reports
. 2013 Mar;20(3):e43-e44.
doi: 10.1111/ene.12044.

Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification

R R Lemos  1 , M F Oliveira  2 , J R M Oliveira  1   3
Affiliations
Case Reports

Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification

R R Lemos et al. Eur J Neurol. 2013 Mar.

Erratum in

  • Eur J Neurol. 2013 Sep;20(9):e117
No abstract available

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References

    1. Wang C, Li Y, Shi L, et al. Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis. Nat Genet 2012; 44: 254-256.
    1. Oliveira JRM. Managing Idiopathic Basal Ganglia Calcification (“Fahr′s Disease”). New York, NY: Nova Publishing, 2012.
    1. Shirahama M, Akiyoshi J, Ishitobi Y, et al. A young woman with visual hallucinations, delusions of persecution and a history of performing arson with possible three-generation Fahr disease. Acta Psychiatr Scand 2010; 121: 75-77.
    1. Maeda K, Idehara R, Nakamura H, Hirai A. Anticipation of familial idiopathic basal ganglia calcification? Intern Med 2012; 51: 987.
    1. Oliveira JRM, Lemos RR, Oliveira MF. Updating genetic studies in familial idiopathic basal ganglia calcification. South Med J 2009; 102: 989.

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