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A new tyrosine hydroxylase genotype associated with early-onset severe encephalopathy.
Giovanniello, Teresa; Claps, Dianella; Carducci, Carla; Carducci, Claudia; Blau, Nenad; Vigevano, Federico; Antonozzi, Italo; Leuzzi, Vincenzo.
Affiliation
  • Giovanniello T; Department of Experimental Medicine, Sapienza Università di Roma, Rome, Italy.
J Child Neurol ; 27(4): 523-5, 2012 Apr.
Article in En | MEDLINE | ID: mdl-21940685
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychomotor Disorders / Tyrosine 3-Monooxygenase / Mutation, Missense Type of study: Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Humans / Male Language: En Journal: J Child Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2012 Document type: Article Affiliation country: Italy
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychomotor Disorders / Tyrosine 3-Monooxygenase / Mutation, Missense Type of study: Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Humans / Male Language: En Journal: J Child Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2012 Document type: Article Affiliation country: Italy