Literature DB >> 27739105

SLC39A14 mutations expand the spectrum of manganese transporter defects causing parkinsonism-dystonia.

Bettina Balint1,2, Kailash P Bhatia1.   

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Year:  2016        PMID： 27739105     DOI： 10.1002/mds.26821

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  2 in total

1.  Frequent lineage-specific substitution rate changes support an episodic model for protein evolution.

Authors:  Neel Prabh; Diethard Tautz
Journal:  G3 (Bethesda)       Date:  2021-12-08       Impact factor: 3.154

2.  Effect of Chelation Therapy on a Korean Patient With Brain Manganese Deposition Resulting From a Compound Heterozygous Mutation in the SLC39A14 Gene.

Authors:  Jae-Hyeok Lee; Jin-Hong Shin
Journal:  J Mov Disord       Date:  2022-03-22
  2 in total

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