Mitochondrial Copy Number and D-Loop Variants in Pompe Patients

OBJECTIVE: Pompe disease is a rare neuromuscular genetic disorder and is classified into two forms of early and late-onset. Over the past two decades, mitochondrial abnor- malities have been recognized as an important contributor to an array of neuromuscular diseases. We therefore aimed to compare m...

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Publicado en:Cell J
Main Authors: Bahreini, Fatemeh, Houshmand, Massoud, Modaresi, Mohammad Hossein, Tonekaboni, Hassan, Nafissi, Shahriar, Nazari, Ferdoss, Akrami, Seyed Mohammad
Formato: Artigo
Idioma:Inglês
Publicado: Royan Institute 2016
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Original Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5011329/
https://ncbi.nlm.nih.gov/pubmed/27602323
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