Osteogénesis Imperfecta: Estudio auditivo y genético de una familia con una mutación en el gen COL1A1.

Leticia Acle-Cervera; Patricia Corriols-Noval; María Teresa Gil-Aguilar; Ana Foltalva-Romero; Carmelo Morales-Angulo

doi:10.14201/orl.19230

Osteogenesis imperfecta: Hearing and genetic study of a family with a mutation in the COL1A1 gene

Leticia Acle-Cervera

Hospital universitario de Torrejón https://orcid.org/0000-0002-8618-4466 leticia_acle[at]hotmail.com
Patricia Corriols-Noval

Hospital Universitario Marqués de Valdecilla https://orcid.org/0000-0001-5440-7330
María Teresa Gil-Aguilar

Hospital Universitario Marqués de Valdecilla https://orcid.org/0000-0002-9952-0764
Ana Foltalva-Romero

Hospital Universitario Marqués de Valdecilla https://orcid.org/0000-0001-7214-0748
Carmelo Morales-Angulo

Hospital Universitario Marqués de Valdecilla https://orcid.org/0000-0002-4268-2762

https://doi.org/10.14201/orl.19230

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How to Cite

Acle-Cervera, L., Corriols-Noval, P., Gil-Aguilar, M. T., Foltalva-Romero, A., & Morales-Angulo, C. (2018). Osteogenesis imperfecta: Hearing and genetic study of a family with a mutation in the COL1A1 gene. Revista ORL, 10(2), 103–108. https://doi.org/10.14201/orl.19230

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Editorial dates

Submitted:

10/07/2018

Acceptance:

10/23/2018

Published:

10/25/2018

Issue

Vol. 10 No. 2 (2019)

Section

Original

Keywords

osteogenesis imperfect
hearing loss
COL1A1 gene
heterogeneity

Supporting agencies

This research didn't have any funding

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