Letter to the Editor
Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype†
Aida Ormazabal and Mercedes Serrano contributed equally to this article. Relevant conflicts of interest/financial disclosures: Nothing to report. Full financial disclosures and author roles may be found in the online version of this article. Support was received from the Biomedical Network Research Centre on Rare Diseases (CIBER-ER, ISCIII), grant FIS PS09/01132, and Agència de Gestió d'Ajuts Universitaris i de Recerca—AGAUR (2009-SGR-00971). Dr. Toma and Dr. Serrano were supported by a CIBER-ER contract and Dr. Artuch by ISCIII (intensificación de la actividad investigadora).
No abstract is available for this article.