Usher syndrome and Nebulin‐associated myopathy in a single patient due to variants in MYO7A and NEB

In a patient with Usher syndrome and atypical muscle complaints, we have identified two separate variants in MYO7A andNEB genes by exome sequencing. The homozygous variants in these two recessive genes could explain the full phenotype of our patient.

Detalles Bibliográficos
Autores principales: Maia, Nuno, Soares, Ana Rita, Fortuna, Ana Maria, Marques, Isabel, Gonçalves, Ana, Santos, Rosário, Melo Pires, Manuel, de Brouwer, Arjan P. M., Jorge, Paula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752365/
https://www.ncbi.nlm.nih.gov/pubmed/33363762
http://dx.doi.org/10.1002/ccr3.3146

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752365/
https://www.ncbi.nlm.nih.gov/pubmed/33363762
http://dx.doi.org/10.1002/ccr3.3146

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