Genetic landscape of primary mitochondrial diseases in children and adults using molecular genetics and genomic investigations of mitochondrial and nuclear genome.

Autor: Ambrose, Anastasia1 (AUTHOR), Bahl, Shalini2,3 (AUTHOR), Sharma, Saloni1 (AUTHOR), Zhang, Dan1 (AUTHOR), Hung, Clara1 (AUTHOR), Jain-Ghai, Shailly1 (AUTHOR), Chan, Alicia1 (AUTHOR), Mercimek-Andrews, Saadet1,4,5,6 (AUTHOR) saadet@ualberta.ca
Zdroj: Orphanet Journal of Rare Diseases. 11/12/2024, Vol. 19 Issue 1, p1-13. 13p.
Databáze: Academic Search Ultimate
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