F. Magrinelli Et Al. , "Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy," MOVEMENT DISORDERS CLINICAL PRACTICE , vol.9, pp.218-228, 2022
Magrinelli, F. Et Al. 2022. Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy. MOVEMENT DISORDERS CLINICAL PRACTICE , vol.9 , 218-228.
Magrinelli, F., Cali, E., Braga, V. L., YİŞ, U., Tomoum, H., Shamseldin, H., ... Raiman, J.(2022). Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy. MOVEMENT DISORDERS CLINICAL PRACTICE , vol.9, 218-228.
Magrinelli, Francesca Et Al. "Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy," MOVEMENT DISORDERS CLINICAL PRACTICE , vol.9, 218-228, 2022
Magrinelli, Francesca Et Al. "Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy." MOVEMENT DISORDERS CLINICAL PRACTICE , vol.9, pp.218-228, 2022
Magrinelli, F. Et Al. (2022) . "Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy." MOVEMENT DISORDERS CLINICAL PRACTICE , vol.9, pp.218-228.
@article{article, author={Francesca Magrinelli Et Al. }, title={Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy}, journal={MOVEMENT DISORDERS CLINICAL PRACTICE}, year=2022, pages={218-228} }