Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study

INTRODUCTION: Moyamoya disease (MMD) is a chronic cerebrovascular steno-occlusive disease of largely unknown etiology. Variants in the RNF213 gene are strongly associated with MMD in East-Asia. In MMD patients of Northern-European origin, no predominant susceptibility variants have been identified s...

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Detalles Bibliográficos
Autores principales: Wiedmann, Markus K.H., Steinsvåg, Ingunn V., Dinh, Tovy, Vigeland, Magnus D., Larsson, Pål G., Hjorthaug, Hanne, Sheng, Ying, Mero, Inger-Lise, Selmer, Kaja K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293314/
https://www.ncbi.nlm.nih.gov/pubmed/37383439
http://dx.doi.org/10.1016/j.bas.2023.101745

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