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[Inborn errors of metabolism as rare diseases with a specific global situation].
An Sist Sanit Navar. 2008;31 Suppl 2:55-73.
An Sist Sanit Navar. 2008.
PMID: 18953372
Free article.
Spanish.
Molecular analysis of hereditary hyperferritinemia-cataract syndrome in a large Basque family.
Pérez de Nanclares G, Castaño L, Martul P, Rica I, Vela A, Sanjurjo P, Aldamiz-Echevarría K, Martínez R, Sarrionandia MJ.
Pérez de Nanclares G, et al. Among authors: aldamiz echevarria k.
J Pediatr Endocrinol Metab. 2001 Mar;14(3):295-300. doi: 10.1515/jpem.2001.14.3.295.
J Pediatr Endocrinol Metab. 2001.
PMID: 11308047
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