Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome.
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| Title: | Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome. |
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| Authors: | Dias CM; Division of Developmental Medicine, Boston Children's Hospital, Boston, MA 02115.; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Department of Pediatrics, Harvard Medical School, Boston, MA 02115.; Department of Pediatrics, Section of Developmental Pediatrics, Section of Genetics and Metabolism, and Denver Fragile X Clinic and Research Center, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO 80045., Issac B; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA 02115., Sun L; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA 02115., Lukowicz A; Department of Pediatrics, Section of Developmental Pediatrics, Section of Genetics and Metabolism, and Denver Fragile X Clinic and Research Center, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO 80045., Talukdar M; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Harvard-Massachusetts Institute of Technology MD/PhD Program, Program in Bioinformatics & Integrative Genomics, Harvard Medical School, Boston, MA 02115., Akula SK; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Harvard-Massachusetts Institute of Technology MD/PhD Program, Program in Neuroscience, Harvard Medical School, Boston, MA 02115., Miller MB; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115., Walsh K; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115., Rockowitz S; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA 02115., Walsh CA; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA 02115.; Department of Pediatrics, Harvard Medical School, Boston, MA 02115.; HHMI, Boston Children's Hospital, Boston, MA 02115.; Department of Neurology, Harvard Medical School, Boston, MA 02115. |
| Source: | Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2023 Jun 06; Vol. 120 (23), pp. e2300052120. Date of Electronic Publication: 2023 May 30. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1091-6490 (Electronic) Linking ISSN: 00278424 NLM ISO Abbreviation: Proc Natl Acad Sci U S A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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