Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Alock S, Malik"'
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 4, Iss C, Pp 62-71 (2017)
Duchenne muscular dystrophy (DMD) is a lethal, X-linked, muscle-wasting disorder caused by mutations in the large, 2.4-Mb dystrophin gene. The majority of DMD-causing mutations are sporadic, multi-exon, frameshifting deletions, with the potential for
Externí odkaz:
https://doaj.org/article/baaed901fbc14b398a47c288c15dcfd1
Autor:
Yafeng, Song, Leon, Morales, Alock S, Malik, Andrew F, Mead, Christopher D, Greer, Marilyn A, Mitchell, Mihail T, Petrov, Leonard T, Su, Margaret E, Choi, Shira T, Rosenblum, Xiangping, Lu, Daniel J, VanBelzen, Ranjith K, Krishnankutty, Frederick J, Balzer, Emanuele, Loro, Robert, French, Kathleen J, Propert, Shangzhen, Zhou, Benjamin W, Kozyak, Peter P, Nghiem, Tejvir S, Khurana, Joe N, Kornegay, Hansell H, Stedman
Publikováno v:
Mol Ther
The essential product of the Duchenne muscular dystrophy (DMD) gene is dystrophin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::191440db6cecb5f5383115a53e99d361
https://pubmed.ncbi.nlm.nih.gov/31653398
https://pubmed.ncbi.nlm.nih.gov/31653398