Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
January 1, 2001Annals of Neurology

A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patients

View Full Paper
Ask AI
Bookmark
Share

Authors

PCP. CoronaThe Neurological InstituteCACarlo AntozziFondazione IRCCS Istituto Neurologico Carlo BestaFCFranco CarraraFondazione IRCCS Istituto Neurologico Carlo Besta

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Corona et al. (2001) studied this question.

synapsesocial.com/papers/6aaba991ae7d76820a16de93https://doi.org/10.1002/1531-8249(200101)49:1<106::aid-ana16>3.0.co;2-t
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Identification of a Novel Mutation in the mtDNA ND5 Gene Associated with MELAS1997 · 171 citations
  2. 2MELAS: Clinical features, biochemistry, and molecular genetics1992 · 510 citations
  3. 3Clinical spectrum of the MELAS mutation in a large pedigree2009 · 55 citations
  4. 4The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS1999 · 118 citations