Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy.

Patients with several inherited human encephalomyopathies exhibit systemic and neurological symptoms in association with specific mitochondrial mutations. The mechanisms by which these mitochondrial mutations result in cellular injury have not been elucidated. One potential cause of neuronal vulnera...

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Bibliografski detalji
Glavni autori: Moudy, A M, Handran, S D, Goldberg, M P, Ruffin, N, Karl, I, Kranz-Eble, P, DeVivo, D C, Rothman, S M
Format: Artigo
Jezik:Inglês
Izdano: 1995
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC42693/
https://ncbi.nlm.nih.gov/pubmed/7846043
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