Genome sequencing identifies three molecular diagnoses including a mosaic variant in the COL2A1 gene in an individual with Pol III–related leukodystrophy and Feingold syndrome

Undiagnosed genetic disease imposes a significant burden on families and health-care resources, especially in cases with a complex phenotype. Here we present a child with suspected leukodystrophy in the context of additional features, including hearing loss, clinodactyly, rotated thumbs, tapered fin...

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Detalles Bibliográficos
Autores principales: Muirhead, Kayla J., Clause, Amanda R., Schlachetzki, Zinayida, Dubbs, Holly, Perry, Denise L., Hagelstrom, R. Tanner, Taft, Ryan J., Vanderver, Adeline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751417/
https://www.ncbi.nlm.nih.gov/pubmed/34737199
http://dx.doi.org/10.1101/mcs.a006143

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751417/
https://www.ncbi.nlm.nih.gov/pubmed/34737199
http://dx.doi.org/10.1101/mcs.a006143

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