دورية أكاديمية
A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder.
العنوان: | A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder. |
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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 |
DOI: | 10.1007/s10803-020-04551-y |
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