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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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Detalhes bibliográficos
Main Authors: Moudy, A M, Handran, S D, Goldberg, M P, Ruffin, N, Karl, I, Kranz-Eble, P, DeVivo, D C, Rothman, S M
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC42693/
https://ncbi.nlm.nih.gov/pubmed/7846043
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