Osteogenesis Imperfecta Due to Compound Heterozygosity for the LEPRE1 Gene

Journal article

Open access

Peer reviewed

Fetal and pediatric pathology, Vol.32(5), pp.319-325

2013-10-01

PMCID: PMC3786543

PMID: 23301918

Abstract

LEPRE 1 gene

osteogenesis imperfecta

Original

perinatal form

autosomal recessive

skeletal dysplasia

url

https://doi.org/10.3109/15513815.2012.754528View

Published (Version of record) Open

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Citation topics: 1 Clinical & Life Sciences; 1.132 Extracellular Matrix & Cell Differentiation; 1.132.1065 Osteogenesis Imperfecta
Web Of Science research areas: Pathology; Pediatrics
ESI research areas: Clinical Medicine

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Source: InCites

Title: Osteogenesis Imperfecta Due to Compound Heterozygosity for the LEPRE1 Gene
Creators: Adrienne Moul - ,
Amanda Alladin - ,
Cristina Navarrete - ,
George Abdenour - ,
Maria M Rodriguez - ,
Publication Details: Fetal and pediatric pathology, Vol.32(5), pp.319-325
Publisher: Informa Healthcare
Academic Unit: Miller School of Medicine; UMMG Department of Pediatrics; UMMG Department of Radiology; UMMG Dept of Pediatrics - Neonatology; UMMG Dept of Pediatrics - Critical Care
Language: English
Resource Type: Journal article
PMID: 23301918
PMCID: PMC3786543
Record Identifier: 991031577212502976