Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families

Despite large sequencing and data sharing efforts, previously characterized pathogenic variants only account for a fraction of Mendelian disease patients, which highlights the need for accurate identification and interpretation of novel variants. In a large Mendelian cohort of 4577 molecularly chara...

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Detalles Bibliográficos
Autores principales: AlAbdi, Lama, Maddirevula, Sateesh, Shamseldin, Hanan E., Khouj, Ebtissal, Helaby, Rana, Hamid, Halima, Almulhim, Aisha, Hashem, Mais O., Abdulwahab, Firdous, Abouyousef, Omar, Alqahtani, Mashael, Altuwaijri, Norah, Jaafar, Amal, Alshidi, Tarfa, Alzahrani, Fatema, Alkuraya, Fowzan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465531/
https://www.ncbi.nlm.nih.gov/pubmed/37644014
http://dx.doi.org/10.1038/s41467-023-40909-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465531/
https://www.ncbi.nlm.nih.gov/pubmed/37644014
http://dx.doi.org/10.1038/s41467-023-40909-3

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