A family with hereditary hyperferritinaemia cataract syndrome : evidence of incomplete penetrance and clinical heterogeneity
- Author
- GONZALEZ-HUERTA, Luz1 ; RAMIREZ-SANCHEZ, Veronica2 ; RIVERA-VEGA, Maria1 ; MESSINA-BAAS, Olga2 ; CUEVAS-COVARRUBIAS, Sergio1
[1] Servicios de Genetica, Universidad Nacional Autonoma de Mexico, Mexico D.F, Mexico
[2] Oftalmologia, Hospital General de Mexico, Facultad de Medicina, Universidad Nacional Autonoma de Mexico, Mexico D.F, Mexico - Source
British journal of haematology. 2008, Vol 143, Num 4, pp 596-598, 3 p ; ref : 1/2 p
- CODEN
- BJHEAL
- ISSN
- 0007-1048
- Scientific domain
- Medical oncology; Hematology
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Hématologie Héréditaire Hétérogénéité Pénétrance génique Cataracte hyperferritinémie syndrome
- Keyword (en)
- Hematology Hereditary Heterogeneity Gene penetrance Hyperferritinemia cataract syndrome
- Keyword (es)
- Hematología Hereditario Heterogeneidad Penetrancia génica
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases
- Discipline
- Blood diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20805488
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1111/j.1365-2141.2008.07345.x 
https://dx.doi.org/10.1111/j.1365-2141.2008.07345.x
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