Parsing heterogeneity in autism spectrum disorder.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Parsing heterogeneity in autism spectrum disorder.
Συγγραφείς: Martín JM; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA., Geschwind DH; Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.; Center for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.; Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.; Institute for Precision Health, University of California Los Angeles, Los Angeles, CA, USA.
Πηγή: Science (New York, N.Y.) [Science] 2026 Sep 17; Vol. 393 (6817), pp. 1188-1189. Date of Electronic Publication: 2026 Sep 17.
Τύπος έκδοσης: News; Comment
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 0404511 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1095-9203 (Electronic) Linking ISSN: 00368075 NLM ISO Abbreviation: Science Subsets: MEDLINE
Imprint Name(s): Publication: : Washington, DC : American Association for the Advancement of Science
Original Publication: New York, N.Y. : [s.n.] 1880-
Ιατρικοί όροι (MeSH): Autism Spectrum Disorder*/genetics , Autism Spectrum Disorder*/physiopathology , Genetic Heterogeneity*, Humans ; Mutation
Περίληψη: Stratifying genetic mutations points to different pathophysiological pathways to a neurodevelopmental disorder.
Σχόλια: Comment on: Science. 2026 Sep 17;393(6817):1250-1257. doi: 10.1126/science.adz6688.. (PMID: 42752124)
Entry Date(s): Date Created: 20260917 Date Completed: 20260917 Latest Revision: 20260921
Update Code: 20260921
DOI: 10.1126/science.ael3062
PMID: 42752156
Βάση Δεδομένων: MEDLINE