Correction To: Novel Mutation G324C in WNT1 Mapped in a Large Pakistani Family With Severe Recessively Inherited Osteogenesis Imperfecta

Journal of Biomedical Science - United Kingdom
doi 10.1186/s12929-019-0525-x
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta

American Journal of Human Genetics
Genetics
2013English

Splints in Severe Osteogenesis Imperfecta.

BMJ
1978English

A Novel De Novo COL1A1 Mutation in a Thai Boy With Osteogenesis Imperfecta Born to Consanguineous Parents

Genetics and Molecular Biology
GeneticsMolecular Biology
2017English

Variable Expressivity of Osteogenesis Imperfecta in a Brazilian Family Due to p.G1079S Mutation in the COL1A1 Gene

Genetics and Molecular Research
MedicineGeneticsMolecular Biology
2012English

A Novel COL1A1 Gene-Splicing Mutation (C.1875+1G>C) in a Brazilian Patient With Osteogenesis Imperfecta

Genetics and Molecular Research
MedicineGeneticsMolecular Biology
2009English

Splice Receptor-Site Mutation C.697-2a>g of the COL1A1 Gene in a Chinese Family With Osteogenesis Imperfecta

Intractable and Rare Diseases Research
Medicine
2019English

Genetics of Nonsyndromic Recessively Inherited Moderate to Severe and Progressive Deafness in Humans

2012English

The Role of Pamidronate in Pediatric Patients With Severe Osteogenesis Imperfecta

Journal of Pediatric Pharmacology and Therapeutics
Child HealthPediatricsPerinatologyPharmacology
2004English

Osteogenesis Imperfecta

2004English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy