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Restless in the mouse cage-A new genetic model for restless legs syndrome: An Editorial Highlight for "Deficiency of Meis1, a transcriptional regulator, in mice and worms:Neurochemical and behavioral characterizations with implications in the restless legs syndrome" on page 522.
Stegmüller, Judith.
Affiliation
  • Stegmüller J; Department of Neurology, RWTH University Hospital, Aachen, Germany.
J Neurochem ; 155(5): 471-474, 2020 12.
Article in En | MEDLINE | ID: mdl-33011998
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Restless Legs Syndrome / Disease Models, Animal / Myeloid Ecotropic Viral Integration Site 1 Protein / Models, Genetic Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: J Neurochem Year: 2020 Document type: Article Affiliation country: Germany Country of publication: United kingdom
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Restless Legs Syndrome / Disease Models, Animal / Myeloid Ecotropic Viral Integration Site 1 Protein / Models, Genetic Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: J Neurochem Year: 2020 Document type: Article Affiliation country: Germany Country of publication: United kingdom