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pro vyhledávání: '"Mia M. Detor"'
Autor:
Jennifer A. Suggs, Girish C. Melkani, Bernadette M. Glasheen, Mia M. Detor, Anju Melkani, Nathan P. Marsan, Douglas M. Swank, Sanford I. Bernstein
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 6, Pp 761-771 (2017)
Individuals with inclusion body myopathy type 3 (IBM3) display congenital joint contractures with early-onset muscle weakness that becomes more severe in adulthood. The disease arises from an autosomal dominant point mutation causing an E706K substit
Externí odkaz:
https://doaj.org/article/0734f576d32c4449a6e56f15badb6a57
