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Fertility Defects in Mice Expressing the L68Q Variant of Human Cystatin C: A ROLE FOR AMYLOID IN MALE INFERTILITY

Hereditary cystatin C amyloid angiopathy is an autosomal dominant disorder in which a variant form of cystatin C (L68Q) readily forms amyloid deposits in cerebral arteries in affected individuals resulting in early death. L68Q protein deposits in human cystatin C amyloid angiopathy patients have als...

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Detalhes bibliográficos
Main Authors: Whelly, Sandra, Serobian, Gaiane, Borchardt, Clinton, Powell, Jonathan, Johnson, Seethal, Hakansson, Katarina, Lindstrom, Veronica, Abrahamson, Magnus, Grubb, Anders, Cornwall, Gail A.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3953282/
https://ncbi.nlm.nih.gov/pubmed/24500719
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M113.515759
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