دورية أكاديمية

A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder.

التفاصيل البيبلوغرافية
العنوان: A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder.
المؤلفون: Graziano C, Despang P, Palombo F, Severi G, Posar A, Cassio A, Pippucci T, Isidori F, Matthes J, Bonora E.
المساهمون: Graziano C, Despang P, Palombo F, Severi G, Posar A, Cassio A, Pippucci T, Isidori F, Matthes J, Bonora E.
سنة النشر: 2021
المجموعة: IRIS Università degli Studi di Bologna (CRIS - Current Research Information System)
مصطلحات موضوعية: Autism spectrum disorder, Genetic, Neurobiology, CACNB2 mutation, Whole exome sequencing
الوصف: Not available.
نوع الوثيقة: article in journal/newspaper
وصف الملف: STAMPA
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32506348; info:eu-repo/semantics/altIdentifier/wos/WOS:000538667400001; volume:51; firstpage:377; lastpage:381; numberofpages:5; journal:JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS; https://hdl.handle.net/11585/776412Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85085963183; https://link.springer.com/article/10.1007/s10803-020-04551-yTest
DOI: 10.1007/s10803-020-04551-y
الإتاحة: https://doi.org/10.1007/s10803-020-04551-yTest
https://hdl.handle.net/11585/776412Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.C755E769
قاعدة البيانات: BASE