Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability

BACKGROUND: Intellectual disability (ID) is a condition that varies widely in both its clinical presentation and its genetic underpinnings. It significantly impacts patients’ learning capacities and lowers their IQ below 70. The solute carrier (SLC) family is the most abundant class of transmembrane...

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Detalles Bibliográficos
Autores principales: Hussain, Syeda Iqra, Muhammad, Nazif, Shah, Salah Ud Din, Fardous, Fardous, Khan, Sher Alam, Khan, Niamatullah, Rehman, Adil U, Siddique, Mehwish, Wasan, Shoukat Ali, Niaz, Rooh, Ullah, Hafiz, Khan, Niamat, Muhammad, Noor, Mirza, Muhammad Usman, Wasif, Naveed, Khan, Saadullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548666/
https://www.ncbi.nlm.nih.gov/pubmed/37794328
http://dx.doi.org/10.1186/s12883-023-03397-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548666/
https://www.ncbi.nlm.nih.gov/pubmed/37794328
http://dx.doi.org/10.1186/s12883-023-03397-y

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