QR Kod

Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review

Abstract Background Pathogenic variants of the AUTS2 (Autism Susceptibility candidate 2) gene predispose to intellectual disability, autism spectrum disorder, attention deficit hyperactivity disorder, facial dysmorphism and short stature. This phenotype is therefore associated with neurocognitive di...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Christophe GAULD, Alice POISSON, Julie REVERSAT, Elodie PEYROUX, Françoise HOUDAYER-ROBERT, Massimiliano ROSSI, Gaetan LESCA, Damien SANLAVILLE, Caroline DEMILY
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMC 2021-07-01
Seri Bilgileri:BMC Psychiatry
Konular:
Online Erişim:https://doi.org/10.1186/s12888-021-03342-8
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!