TY  - GEN

T1  - Biallelic mutations in SUPV3L1 cause an inherited neurodevelopmental disorder with variable leukodystrophy due to aberrant mitochondrial double stranded RNA processing

T2  - Research Square Platform LLC

UR  - http://dx.doi.org/10.21203/rs.3.rs-4356120/v1

PY  - 2024/05/10

AU  - Green L

AU  - Hamilton N

AU  - Elpidorou M

AU  - Maroofian R

AU  - Douglas AGL

AU  - Õunap K

AU  - Rose AMS

AU  - Harris EL

AU  - Elworthy S

AU  - Renshaw SA

AU  - Low EC et al

ED  - 

DO  - DOI: 10.21203/rs.3.rs-4356120/v1

Y2  - 2024/12/22

ER  -