Literature DB >> 21112252

Infantile parkinsonism-dystonia due to dopamine transporter gene mutations: another genetic twist.

Craig Blackstone1.   

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Year:  2010        PMID: 21112252     DOI: 10.1016/S1474-4422(10)70280-5

Source DB:  PubMed          Journal:  Lancet Neurol        ISSN: 1474-4422            Impact factor:   44.182


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  2 in total

1.  Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood.

Authors:  Joanne Ng; Juan Zhen; Esther Meyer; Kevin Erreger; Yan Li; Naseebullah Kakar; Jamil Ahmad; Holger Thiele; Christian Kubisch; Nicholas L Rider; D Holmes Morton; Kevin A Strauss; Erik G Puffenberger; Daniela D'Agnano; Yair Anikster; Claudia Carducci; Keith Hyland; Michael Rotstein; Vincenzo Leuzzi; Guntram Borck; Maarten E A Reith; Manju A Kurian
Journal:  Brain       Date:  2014-03-10       Impact factor: 13.501

Review 2.  What is new for monoamine neurotransmitter disorders?

Authors:  Clara Marecos; Joanne Ng; Manju A Kurian
Journal:  J Inherit Metab Dis       Date:  2014-04-03       Impact factor: 4.982

  2 in total

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