Results 161 to 168 of about 3,944 (168)

Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant

Neuromuscular Disorders, 2020
Alice Abdel Aleem, Omer F Kuzu, Omar Osman   +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
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  

MUTATIONS IN LAMA2 GENE OF ZEBRAFISH

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

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  

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

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

THERAPEUTIC LAMA2 PAYLOAD FOR TREATMENT OF CONGENITAL MUSCULAR DYSTROPHY

2022
GUELL CARGOL MARC, SANCHEZ-MEJIAS GARCIA AVENCIA, PALLARES MASMITJA MARIA   +2 more
openaire   +1 more source

Modelling LAMA2-CMD to explore physiopathology and therapeutic options

Caron, Leslie, V, Allamand
openaire   +1 more source