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eNauka >  Results >  Characterization of GNB1 mutations as a cause of global developmental delay in combination with dystonia, ataxia, or chorea in children
Title: Characterization of GNB1 mutations as a cause of global developmental delay in combination with dystonia, ataxia, or chorea in children
Authors: H. Baumann; I. Masuho; D. Patil; S. Steinrücke; E. Hebert; V. Dobričić; I. Hüning; G. Gillessen-Kaesbach; A. Westenberger; Savić Pavićević, Dušanka Lj.  ;
Issue Date: 2017
Publication: 21st International Congress of Parkinson's disease and movement disorders, Movement Disorders
ISSN: 1531-8257 Movement Disorders Search Idenfier
Publisher: International Parkinson and Movement Disorder Society, Vankuver
Type: Conference Paper
Collation: vol. 32 br. suppl 2 str. 439-439
URI: https://enauka.gov.rs/handle/123456789/224339
URL: http://www.mdsabstracts.org/abstract/characterization-of-gnb1-mutations-as-a-cause-of-global-developmental-delay-in-combination-with-dystonia-ataxia-or-chorea-in-children/
Metadata source: Migrirano iz RIS podataka
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