Wikidata

(Q53567971)

English

A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site.

scientific article published in July 2007

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Statements

title
A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site. (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17579362
retrieved
15 May 2018
reference URL
http://europepmc.org/abstract/MED/17579362

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