Cortical connectivity in the face of congenital structural changes—A case of homozygous LAMC3 mutation

The homozygous LAMC3 gene mutation is associated with severe bilateral smoothening and thickening of the lateral occipital cortex . Despite this and further significant changes in gray matter structure, a patient harboring this mutation exhibited a range of remarkably intact perceptual abilities . O...

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Detalles Bibliográficos
Autores principales: Demirayak, Pinar, Karli Oguz, Kader, Ustun, Fatma Seyhun, Urgen, Buse Merve, Topac, Yasemin, Gilani, Irtiza, Kansu, Tulay, Saygi, Serap, Ozcelik, Tayfun, Boyaci, Huseyin, Doerschner, Katja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413815/
https://www.ncbi.nlm.nih.gov/pubmed/34124859
http://dx.doi.org/10.1002/brb3.2241

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413815/
https://www.ncbi.nlm.nih.gov/pubmed/34124859
http://dx.doi.org/10.1002/brb3.2241

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