[DMD gene--the largest human gene]
- PMID: 1461839
[DMD gene--the largest human gene]
Similar articles
-
[Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene].Minerva Pediatr. 1991 Mar;43(3):67-70. Minerva Pediatr. 1991. PMID: 1870528 Italian. No abstract available.
-
Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family.Hum Mutat. 1994;3(2):133-40. doi: 10.1002/humu.1380030208. Hum Mutat. 1994. PMID: 8199594
-
Dystrophin deficiency in a case of congenital myopathy.J Neurol. 1992 Feb;239(2):76-8. doi: 10.1007/BF00862976. J Neurol. 1992. PMID: 1552307
-
[Regulation of human DMD gene expression. An example of multiple utilization of genetic information].Postepy Biochem. 1998;44(1):48-55. Postepy Biochem. 1998. PMID: 9738237 Review. Polish. No abstract available.
-
[Dystrophinopathies: concept and diagnostic methodology].Neurologia. 1994 May;9(5):191-7. Neurologia. 1994. PMID: 8024825 Review. Spanish. No abstract available.
Cited by
-
Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report.BMC Med Genet. 2020 Nov 11;21(1):222. doi: 10.1186/s12881-020-01157-0. BMC Med Genet. 2020. PMID: 33176713 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical