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Autor:
M, Marini, A A, Salmi, M S, Watihayati, M D, SMardziah, M K, Zahri, B P, Hoh, R, Ankathil, P S, Lai, B A, Zilfalil
Publikováno v:
The Medical journal of Malaysia. 63(1)
Duchenne Muscular Dystrophy (DMD) is an X-linked recessive genetic disorder characterized by rapidly progressive muscle weakness. The disease is caused by deletion, duplication or point mutation of the dystrophin gene, located on the X chromosome (Xp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73841ff7660fea4f973a8bd74ca7a588
https://pubmed.ncbi.nlm.nih.gov/18935728
https://pubmed.ncbi.nlm.nih.gov/18935728
