Work

Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene

Year: 2009

Type: article

Source: Movement Disorders

DOI: 10.1002/mds.22455

Authors: Diane Doummar, Fabienne Clot, Marie Vidailhet, Alexandra Afenjar, Alexandra Durr, Alexis Brice, Cyril Mignot, Agnès Guet, Thierry Billette de Villemeur, Diana Rodriguez

Institutions: Hôpital Armand-Trousseau, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Inserm, Université Pierre-et-Marie-Curie

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

OpenAlex ID: W2137703691

FWCI: 0.425

Cites: 8

Cited by: 7

Related to: 10