Publications by authors named "Leticia Olavarrieta"

7Publications

Mutation affecting the proximal promoter of Endoglin as the origin of hereditary hemorrhagic telangiectasia type 1.

BMC Med Genet 2017 Feb 23;18(1):20. Epub 2017 Feb 23.

Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Ramiro de Maeztu 9, Madrid, 28040, Spain.

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February 2017

Relevance of complement factor H-related 1 (CFHR1) genotypes in age-related macular degeneration.

Invest Ophthalmol Vis Sci 2012 Mar 1;53(3):1087-94. Epub 2012 Mar 1.

Department of Cellular and Molecular Medicine, Centro de Investigaciones Biológicas (CSIC) and Ciber de Enfermedades Raras (CIBERER), Madrid, Spain.

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March 2012

Characterization of a spontaneous, recessive, missense mutation arising in the Tecta gene.

J Assoc Res Otolaryngol 2008 Jun 2;9(2):202-14. Epub 2008 May 2.

Unidad de Genética Molecular, Hospital Ramón y Cajal, Carretera de Colmenar Km 9, 28034, Madrid, Spain.

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June 2008