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Study of a fetal brain affected by a severe form of tyrosine hydroxylase deficiency, a rare cause of early parkinsonism

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Year: 2015
Type: article
Source: Metabolic Brain Disease
DOI: 10.1007/s11011-015-9780-z
Authors: Alba Tristán-Noguero, Héctor Díez, Cristina Jou, Mercè Pineda, Aida Ormazábal, Aurora Sánchez, Rafael Artuch, Àngels Garcia-Cazorla
Institutions: Hospital Sant Joan de Déu Barcelona, Instituto de Salud Carlos III, Centre for Biomedical Network Research on Rare Diseases, Hospital Clínic de Barcelona, Consorci Institut D'Investigacions Biomediques August Pi I Sunyer
Language: English

Topic: Metabolism and Genetic Disorders
Subfield: Clinical Biochemistry
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funder: Instituto de Salud Carlos III
Award: G1605045296
OpenAlex ID: W2299414019
FWCI: 0.219
Cites: 15
Cited by: 11
Related to: 10
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