Cargando…
A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a devastating progressive motor neuron disease that affects people of all ethnicities. Approximately 90% of ALS cases are sporadic and thought to have multifactorial pathogenesis. To understand the genetics of sporadic ALS, we conducted a genome-wide associatio...
Ejemplares similares
-
The SYNGAP1 3′UTR Variant in ALS Patients Causes Aberrant SYNGAP1 Splicing and Dendritic Spine Loss by Recruiting HNRNPK
por: Yokoi, Satoshi, et al.
Publicado: (2022) -
Acute Unilateral Isolated Oculomotor Nerve Palsy in an Adult Patient with Influenza A
por: Senda, Joe, et al.
Publicado: (2018) -
Nivolumab for the treatment of malignant melanoma in a patient with pre-existing myasthenia gravis
por: Maeda, Osamu, et al.
Publicado: (2016) -
High-Resolution Melting (HRM) Analysis of the Cu/Zn Superoxide Dismutase (SOD1) Gene in Japanese Sporadic Amyotrophic Lateral Sclerosis (SALS) Patients
por: Akimoto, Chizuru, et al.
Publicado: (2011) -
Semantic deficits in ALS related to right lingual/fusiform gyrus network involvement
por: Ogura, Aya, et al.
Publicado: (2019)