Novel mutation of FKBP10 in a pediatric patient with osteogenesis imperfecta type XI identified by clinical exome sequencing

Novel mutation of FKBP10 in a pediatric patient with osteogenesis imperfecta type XI identified by clinical exome sequencing

Harvy Mauricio Velasco,1,2 Jessica L Morales2 1Master of Human Genetics, National University of Colombia and Geneticist in Central Military Hospital, Bogotá DC, Colombia; 2Faculty of Medicine, Universidad Nacional de Colombia, Bogotá DC, Colombia Abstract: Osteogenesis imperfec...

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Bibliographic Details
Main Authors: Velasco HM, Morales JL
Format: Article
Language:English
Published: Dove Medical Press 2017-11-01
Series:The Application of Clinical Genetics
Subjects:
Osteogenesis imperfecta type XI
FKBP 10
diagnostic odyssey.
Online Access:https://www.dovepress.com/novel-mutation-of-fkbp10-in-a-pediatric-patient-with-osteogenesis-impe-peer-reviewed-article-TACG

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https://www.dovepress.com/novel-mutation-of-fkbp10-in-a-pediatric-patient-with-osteogenesis-impe-peer-reviewed-article-TACG

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