A knock-in mouse model for the R120G mutation of alphaBcrystallin recapitulates human hereditary myopathy and cataracts

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Autoria(s): Andley, Usha P; Hamilton, Paul D; Ravi, Nathan; Weihl, Conrad C

Data(s)	01/01/2011
Formato	application/pdf
Identificador	http://digitalcommons.wustl.edu/open_access_pubs/552 http://digitalcommons.wustl.edu/cgi/viewcontent.cgi?article=1552&context=open_access_pubs
Publicador	Digital Commons@Becker
Fonte	Open Access Publications
Palavras-Chave	#Medicine and Health Sciences
Tipo	text