Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndrome

BACKGROUND: Stickler syndrome (STL) is a rare, clinically and molecularly heterogeneous connective tissue disorder. Pathogenic variants occurring in a variety of genes cause STL, mainly inherited in an autosomal dominant fashion. Autosomal recessive STL is ultra-rare with only four families with bia...

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Detalles Bibliográficos
Autores principales: Rad, Aboulfazl, Najafi, Maryam, Suri, Fatemeh, Abedini, Soheila, Loum, Stephen, Karimiani, Ehsan Ghayoor, Daftarian, Narsis, Murphy, David, Doosti, Mohammad, Moghaddasi, Afrooz, Ahmadieh, Hamid, Sabbaghi, Hamideh, Rajati, Mohsen, Hashemi, Narges, Vona, Barbara, Schmidts, Miriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892745/
https://www.ncbi.nlm.nih.gov/pubmed/35241111
http://dx.doi.org/10.1186/s13023-022-02244-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892745/
https://www.ncbi.nlm.nih.gov/pubmed/35241111
http://dx.doi.org/10.1186/s13023-022-02244-6

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