Answer to Gerber et al. “Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy”

Gal et al address the issues raised by Gerber et al and reiterate that patients in their study showed decreased Misato homolog 1 (MSTO1) mRNA and protein levels, but also confirm finding of Gerber et al that the mutation is in MSTO2p pseudogene. Whether MSTO2p variant contributes to the observed dec...

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Detalles Bibliográficos
Autores principales: Gál, Anikó, Santos, Janine H, Molnár, Mária Judit, Hajnóczky, György
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405052/
https://www.ncbi.nlm.nih.gov/pubmed/37431815
http://dx.doi.org/10.15252/emmm.202216251

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405052/
https://www.ncbi.nlm.nih.gov/pubmed/37431815
http://dx.doi.org/10.15252/emmm.202216251

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