Showing results (771-780 of 861) with videos related to
Sort By:
Pageof 87
Neurology. Genetics|September 14, 2019
Erratum: Genome-wide Brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson diseaseNeurology. Genetics|February 12, 2021
DMPK mRNA Expression in Human Brain Tissue Throughout the LifespanKathleen E Langbehn, Zoe Carlson-Stadler, Ellen van der Plas, et al.Neurology. Genetics|February 12, 2021
C9orf72 and the Care of the Patient With ALS or FTD: Progress and Recommendations After 10 YearsJennifer RoggenbuckNeurology. Genetics|October 22, 2016
Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)S T Oestergaard, T Stojkovic, J R Dahlqvist, et al.Neurology. Genetics|November 11, 2016
FHF1 (FGF12) epileptic encephalopathySameer Al-Mehmadi, Miranda Splitt, , et al.Neurology. Genetics|November 11, 2016
Copy number analysis reveals a novel multiexon deletion of the COLQ gene in congenital myastheniaWei Wang, Yanhong Wu, Chen Wang, et al.Neurology. Genetics|March 8, 2019
Genotype-structure-phenotype relationships diverge in paralogs ATP1A1, ATP1A2, and ATP1A3Kathleen J Sweadner, Elena Arystarkhova, John T Penniston, et al.Neurology. Genetics|March 8, 2019
GNE genotype explains 20% of phenotypic variability in GNE myopathyOksana Pogoryelova, Ian J Wilson, Hank Mansbach, et al.Neurology. Genetics|March 8, 2019
Erratum: The complex structure of ATXN2 genetic variationNeurology. Genetics|August 13, 2019
MAPT p.V363I mutation: A rare cause of corticobasal degenerationSarah Ahmed, Monica Diez Fairen, Marya S Sabir, et al.Pageof 87