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An atypical expression of core α-Dystroglycan and Laminin-α2 in skin fibroblasts of patients with congenital muscular dystrophies.
Sabry, Sahar; Issa, Mahmoud Y; Abdel-Hamid, Mohamed S; Eissa, Noura R; Abdel-Ghafar, Sherif F; Ibrahim, Mona M; Zaki, Maha S.
Affiliation
  • Sabry S; Biochemical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre (NRC), Cairo, Egypt. sas_pharmacienne@yahoo.com.
  • Issa MY; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre (NRC), Cairo, Egypt.
  • Abdel-Hamid MS; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre (NRC), Cairo, Egypt.
  • Eissa NR; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre (NRC), Cairo, Egypt.
  • Abdel-Ghafar SF; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre (NRC), Cairo, Egypt.
  • Ibrahim MM; Biochemical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre (NRC), Cairo, Egypt.
  • Zaki MS; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre (NRC), Cairo, Egypt.
Mol Biol Rep ; 50(8): 6373-6379, 2023 Aug.
Article in En | MEDLINE | ID: mdl-37318662
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Laminin / Muscular Dystrophies Limits: Humans Language: En Journal: Mol Biol Rep Year: 2023 Document type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Laminin / Muscular Dystrophies Limits: Humans Language: En Journal: Mol Biol Rep Year: 2023 Document type: Article