Unexplored regulatory sequences of divergently paired GLA and HNRNPH2 loci pertinent to Fabry disease in human kidney and skin cells: Presence of an active bidirectional promoter

Fabry disease (FD) is a rare hereditary disorder characterized by a wide range of symptoms caused by a variety of mutations in the galactosidase α (GLA) gene. The heterogeneous nuclear ribonucleoprotein (HNRNPH2) gene is divergently paired with GLA on chromosome X and is thought to be implicated in...

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Detalles Bibliográficos
Autores principales: Al-Obaide, Mohammed A. Ibrahim, Al-Obaidi, Ibtisam I., Vasylyeva, Tetyana L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792484/
https://www.ncbi.nlm.nih.gov/pubmed/33456521
http://dx.doi.org/10.3892/etm.2020.9586

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792484/
https://www.ncbi.nlm.nih.gov/pubmed/33456521
http://dx.doi.org/10.3892/etm.2020.9586

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