Establishment of Mouse Model of MYH9 Disorders: Heterozygous R702C Mutation Provokes Macrothrombocytopenia with Leukocyte Inclusion Bodies, Renal Glomerulosclerosis and Hearing Disability

Nonmuscle myosin heavy chain IIA (NMMHCIIA) encoded by MYH9 is associated with autosomal dominantly inherited diseases called MYH9 disorders. MYH9 disorders are characterized by macrothrombocytopenia and very characteristic inclusion bodies in granulocytes. MYH9 disorders frequently cause nephritis,...

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Detalhes bibliográficos
Main Authors: Suzuki, Nobuaki, Kunishima, Shinji, Ikejiri, Makoto, Maruyama, Shoichi, Sone, Michihiko, Takagi, Akira, Ikawa, Masahito, Okabe, Masaru, Kojima, Tetsuhito, Saito, Hidehiko, Naoe, Tomoki, Matsushita, Tadashi
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3748045/
https://ncbi.nlm.nih.gov/pubmed/23976996
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0071187
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