Novel mouse models of oculopharyngeal muscular dystrophy (OPMD) reveal early onset mitochondrial defects and suggest loss of PABPN1 may contribute to pathology. (Q50962265)

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Novel mouse models of oculopharyngeal muscular dystrophy (OPMD) reveal early onset mitochondrial defects and suggest loss of PABPN1 may contribute to pathology.
scientific article

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    title
    Novel mouse models of oculopharyngeal muscular dystrophy (OPMD) reveal early onset mitochondrial defects and suggest loss of PABPN1 may contribute to pathology. (English)
    1 reference
    stated in
    Europe PubMed Central
    PubMed publication ID
    28575395
    retrieved
    26 March 2018
    reference URL
    http://europepmc.org/abstract/MED/28575395
    author name string

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