Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy

PURPOSE: Lamins are the major component of nuclear lamina, maintaining structural integrity of the nucleus. Lamin A/C variants are well established to cause a spectrum of disorders ranging from myopathies to progeria, termed laminopathies. Phenotypes resulting from variants in LMNB1 and LMNB2 have b...

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Detalles Bibliográficos
Autores principales: Parry, David A., Martin, Carol-Anne, Greene, Philip, Marsh, Joseph A., Blyth, Moira, Cox, Helen, Donnelly, Deirdre, Greenhalgh, Lynn, Greville-Heygate, Stephanie, Harrison, Victoria, Lachlan, Katherine, McKenna, Caoimhe, Quigley, Alan J., Rea, Gillian, Robertson, Lisa, Suri, Mohnish, Jackson, Andrew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2020
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862057/
https://www.ncbi.nlm.nih.gov/pubmed/33033404
http://dx.doi.org/10.1038/s41436-020-00980-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862057/
https://www.ncbi.nlm.nih.gov/pubmed/33033404
http://dx.doi.org/10.1038/s41436-020-00980-3

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