Biallelic MFSD2 Avariants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features. (2020)

First Author: Scala M.

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

No abstract provided

Type: Conference/Paper/Proceeding/Abstract

Volume: 28

Parent Publication: EUROPEAN JOURNAL OF HUMAN GENETICS

Issue: SUPPL 1

ISSN: 1018-4813