A Single-Nucleotide Polymorphism in Serine-Threonine Kinase 11, the Gene Encoding Liver Kinase B1, Is a Risk Factor for Multiple Sclerosis

We identified a family in which five siblings were diagnosed with multiple sclerosis (MS) or clinically isolated syndrome. Several women in the maternal lineage have comorbidities typically associated with Peutz Jeghers Syndrome, a rare autosomal-dominant disease caused by mutations in the serine-th...

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Detalles Bibliográficos
Autores principales: Boullerne, Anne I., Skias, Demetrios, Hartman, Elizabeth M., Testai, Fernando D., Kalinin, Sergey, Polak, Paul E., Feinstein, Douglas L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342367/
https://www.ncbi.nlm.nih.gov/pubmed/25694554
http://dx.doi.org/10.1177/1759091415568914

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4342367/
https://www.ncbi.nlm.nih.gov/pubmed/25694554
http://dx.doi.org/10.1177/1759091415568914

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