Congenital muscular dystrophy type 1A with residual merosin expression
Hyo Jeong Kim (Kim HJ), Young-Chul Choi (Choi YC), Hyung Jun Park (Park HJ), Young-Mock Lee (Lee YM), Heung Dong Kim (Kim HD), Joon Soo Lee (Lee JS), Hoon-Chul Kang (Kang HC)
Clin Exp Pediatr. 2014;57(3):149-152. Published online 2014 Mar 31 DOI: https://doi.org/10.3345/kjp.2014.57.3.149
|
Citations to this article as recorded by
Dystroglycanopathies: Genetic Bases of Muscular Dystrophies Due to Alteration in the O-Glycosylation of α-Dystroglycan
M.A. Cubilla, G.M. Papazoglu, C.G. Asteggiano
Journal of Inborn Errors of Metabolism and Screeni.2023;[Epub] CrossRef An atypical expression of core α-Dystroglycan and Laminin-α2 in skin fibroblasts of patients with congenital muscular dystrophies
Sahar Sabry, Mahmoud Y Issa, Mohamed S Abdel-Hamid, Noura R Eissa, Sherif F Abdel-Ghafar, Mona M Ibrahim, Maha S Zaki
Molecular Biology Reports.2023; 50(8): 6373. CrossRef Prenatal Diagnosis of Merosin-Deficient Muscular Dystrophy
Erdem Fadiloglu, Gonca Ozten, Canan Unal, Beril Talim, Haluk Topaloglu, Mehmet Sinan Beksac
Fetal and Pediatric Pathology.2018; 37(6): 418. CrossRef
|