Reply

dc.contributor.author	Shenasi, A
dc.contributor.author	Fouladi, RF
dc.date.accessioned	2018-08-26T09:33:43Z
dc.date.available	2018-08-26T09:33:43Z
dc.date.issued	2008
dc.identifier.uri	http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/57619
dc.description.abstract	[No abstract available]
dc.language.iso	English
dc.relation.ispartof	Nephrology Dialysis Transplantation
dc.subject	gelsolin
dc.subject	amyloidosis
dc.subject	autosomal dominant inheritance
dc.subject	blindness
dc.subject	chromosome 9q
dc.subject	developing country
dc.subject	family study
dc.subject	gene locus
dc.subject	gene mutation
dc.subject	human
dc.subject	Iran
dc.subject	Ireland
dc.subject	letter
dc.subject	mental stress
dc.subject	perception deafness
dc.subject	priority journal
dc.subject	rare disease
dc.subject	retinitis pigmentosa
dc.title	Reply
dc.type	Article
dc.citation.volume	23
dc.citation.issue	3
dc.citation.spage	1071
dc.citation.epage	1072
dc.citation.index	Scopus
dc.identifier.DOI	https://doi.org/10.1093/ndt/gfm586

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