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Publications by Maria José Perez-Lucena
On the Hyperferritinemia and Hereditary Cataract Syndrome
Open Journal of Blood Diseases
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Homozygous Mutation of the 5'UTR Region of the L-Ferritin Gene in the Hereditary Hyperferritinemia Cataract Syndrome and Its Impact on the Phenotype
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Clinical Features and Molecular Analysis of Seven British Kindreds With Hereditary Hyperferritinaemia Cataract Syndrome
European Journal of Human Genetics
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Cataract-Deafness-Hypogonadism Syndrome
Calpain May Contribute to Hereditary Cataract Formation in Sheep
Investigative Ophthalmology and Visual Science
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Hereditary Breast and Ovarian Cancer Syndrome
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Cataract Associated With an Hereditary Retinal Lesion in Rats
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Hereditary Cup-Shaped Ears and the Pierre Robin Syndrome.
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SMAD4 Mutation and the Combined Syndrome of Juvenile Polyposis Syndrome and Hereditary Haemorrhagic Telangiectasia
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Hereditary C1q Deficiency and Secondary Sjogren's Syndrome
Annals of the Rheumatic Diseases
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