Citation Tools

Download PDFPDF
Short Report
A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features

Download to a citation manager

Cite this article as:
Marin-Valencia I, Novarino G, Johansen A, et al
A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features