Literature DB >> 8639868

Molecular basis for the hereditary hyperferritinemia-cataract syndrome.

D Girelli, O Olivieri, P Gasparini, R Corrocher.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1996        PMID： 8639868

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


× No keyword cloud information.
  2 in total

Review 1.  Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder.

Authors:  Gunda Millonig; Martina U Muckenthaler; Sebastian Mueller
Journal:  Hum Genomics       Date:  2010-04       Impact factor: 4.639

2.  Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract.

Authors:  Thomas M Bennett; Giovanni Maraini; Chongfei Jin; Wenmin Sun; J Fielding Hejtmancik; Alan Shiels
Journal:  Mol Vis       Date:  2013-04-11       Impact factor: 2.367
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.