BIBLIOGRAPHIC RECORD
Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia
This record contains bibliographic metadata. Open the linked source to check the work; the record does not include its full text.
- Recorded authors
- Manju A. Kurian; Juan Zhen; Shuyuan Cheng; Yan Li; Santosh Mordekar; Philip E. Jardine; Neil V. Morgan; Esther Meyer; Louise J. Tee; Shanaz S. Pasha; Evangeline Wassmer; Simon Heales; Paul Gissen; Maarten E. A. Reith; Eamonn Richard Maher
- Source of metadata
- OpenAlex
- Year recorded
- 2009
Public identifiers and source
Open the source recordReference
Manju A. Kurian; Juan Zhen; Shuyuan Cheng; Yan Li; Santosh Mordekar; Philip E. Jardine; Neil V. Morgan; Esther Meyer; Louise J. Tee; Shanaz S. Pasha; Evangeline Wassmer; Simon Heales; Paul Gissen; Maarten E. A. Reith; Eamonn Richard Maher. (2009). Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia. https://openalex.org/W2093003543
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Permanent record URL: https://brain.psiconautica.org/en/documentos/d-41cdedbe8d64718e19dff3666c37794a/