Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous system

Overview of attention for article published in Orphanet Journal of Rare Diseases, January 2018

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RT @Biblioteca_SJD: Hypermanganesemia due to mutations in SLC39A14: further insights into Mn; deposition in the central nervous system http…

Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous system. https://t.co/b2BZfRlZrF

RT @Biblioteca_SJD: Hypermanganesemia due to mutations in SLC39A14: further insights into Mn; deposition in the central nervous system https://t.co/vSvSbVqegI #PublicaSJDBarcelona

RT @Biblioteca_SJD: Hypermanganesemia due to mutations in SLC39A14: further insights into Mn; deposition in the central nervous system https://t.co/zhMudJri2v #PublicaSJDBarcelona

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