LMNB1

Publications

Cristofoli F et al. De novo variants in the LMNB1 gene cause pronounced syndromic microcephaly and disruption of nuclear envelope integrity. Am. J. Hum. Genet. 2020; 107(4):753-762. PMID: 32910914

Parry DA et al. Heterozygouslamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy. Genet. Med. 2020 Online ahead of print. PMID: 33033404