Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy

INTRODUCTION: Protein aggregation is a common cause of neuropathology. The protein aggregation myopathy Limb-Girdle Muscular Dystrophy 1D (LGMD1D) is caused by mutations of amino acids Phe89 or Phe93 of DNAJB6, a co-chaperone of the HSP70 anti-aggregation protein. Another DNAJB6 mutation, Pro96Arg,...

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Библиографические подробности
Опубликовано в: :Acta Neuropathol Commun
Главные авторы: Ruggieri, Alessandra, Brancati, Francesco, Zanotti, Simona, Maggi, Lorenzo, Pasanisi, Maria Barbara, Saredi, Simona, Terracciano, Chiara, Antozzi, Carlo, D′Apice, Maria Rosaria, Sangiuolo, Federica, Novelli, Giuseppe, Marshall, Christian R., Scherer, Stephen W., Morandi, Lucia, Federici, Luca, Massa, Roberto, Mora, Marina, Minassian, Berge A.
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2015
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Research
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4513909/
https://ncbi.nlm.nih.gov/pubmed/26205529
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-015-0224-0
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