Results 121 to 130 of about 3,643 (133)

Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophy

Brain and Development, 2016
, Juan Ding, Renqian Du
exaly  

Brain Dysfunction in LAMA2-Related Congenital Muscular Dystrophy: Lessons From Human Case Reports and Mouse Models

Frontiers in Molecular Neuroscience, 2020
Holly Colognato
exaly  

Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy

Scientific Reports, 2018
, Ling Zhang, Juan Ding
exaly  

MUTATIONS IN LAMA2 GENE OF ZEBRAFISH

2008
HALL THOMAS EDWARD, BRYSON-RICHARDSON ROBERT JAMES, CURRIE PETER DAVID   +2 more
openaire   +1 more source

Amelioration of Muscle and Nerve Pathology in LAMA2 Muscular Dystrophy by AAV9-Mini-Agrin

Molecular Therapy - Methods and Clinical Development, 2018
Yi Dai, Quan Jin, Bin Xiao
exaly  

LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients

Clinical Genetics, 2008
Isabel Soares-Silva, Elsa Bronze-Da-Rocha, Clara Barbot   +2 more
exaly  

Clinical and molecular characterization of limb‐girdle muscular dystrophy due to LAMA2 mutations

Muscle and Nerve, 2011
John Vissing, Gianni Sorarù, Luca Bello   +2 more
exaly  

Controversial opinion: evaluation of EGR1 and LAMA2 loci for high myopia in Chinese populations

Journal of Zhejiang University: Science B, 2016
Wei Han, Zhu Huang
exaly  

Phenotypic variability of myopathies associated with LAMA2 gene mutations

European Journal of Paediatric Neurology, 2017
Filipe Palavra, Carmen Costa, Vera Ribeiro, Henriqueta Araújo, Isabel Fineza   +4 more
openaire   +1 more source

LAMA2, PLXDC2 AND MLL4 AS NOVEL BIOMARKERS FOR PREDIABETES AND DIABETES

2020
YANG WEN-CHIN, YANG MENG-TING
openaire   +4 more sources