Cargando…
Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta
Autores principales: | Kausar, Mehran, Siddiqi, Saima, Yaqoob, Muhammad, Mansoor, Sajid, Makitie, Outi, Mir, Asif, Khor, Chiea Chuen, Foo, Jia Nee, Anees, Mariam |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487057/ https://www.ncbi.nlm.nih.gov/pubmed/31030663 http://dx.doi.org/10.1186/s12929-019-0525-x |
Ejemplares similares
-
Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta
por: Kausar, Mehran, et al.
Publicado: (2018) -
A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family
por: Kausar, Mehran, et al.
Publicado: (2019) -
Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family
por: Ajmal, Muhammad, et al.
Publicado: (2017) -
Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds
por: Kausar, Mehran, et al.
Publicado: (2022) -
Fatigue and disturbances of sleep in patients with osteogenesis imperfecta – a cross-sectional questionnaire study
por: Arponen, Heidi, et al.
Publicado: (2018)