Literature DB >> 21465550

Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype.

Aida Ormazabal, Mercedes Serrano, Angels Garcia-Cazorla, Jaume Campistol, Rafael Artuch, Pedro Castro de Castro, Estíbaliz Barredo-Valderrama, Judith Armstrong, Claudio Toma, Bru Cormand.   

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Year:  2011        PMID： 21465550     DOI： 10.1002/mds.23564

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


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  2 in total

Review 1.  Tyrosine hydroxylase gene: another piece of the genetic puzzle of Parkinson's disease.

Authors:  Guney Bademci; Jeffery M Vance; Liyong Wang
Journal:  CNS Neurol Disord Drug Targets       Date:  2012-06-01       Impact factor: 4.388

Review 2.  Genetics of monoamine neurotransmitter disorders.

Authors:  Wai-Kwan Siu
Journal:  Transl Pediatr       Date:  2015-04
  2 in total

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