The authors of "<Emphasis Type='Italic'>MSTO1</Emphasis> mutations…" (https://t.co/8ADmb8LnIg) included RRIDs in their paper! RRIDs like this improve reproducibility in scientific research. #OpenScience #accelerateopenscience
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. https://t.co/Os0DAkD7XA
RT @MitoMORPH: Two new papers from PhD Phenom Rasha @rsabouny in the ShuttLab @MitoMORPH, looking at mtDNA depletion when mitochondrial fus…
RT @MitoMORPH: Two new papers from PhD Phenom Rasha @rsabouny in the ShuttLab @MitoMORPH, looking at mtDNA depletion when mitochondrial fus…
RT @MitoMORPH: Two new papers from PhD Phenom Rasha @rsabouny in the ShuttLab @MitoMORPH, looking at mtDNA depletion when mitochondrial fus…
RT @rsabouny: Second paper from ShuttLab @MitoMORPH this month! International collaboration comprising the largest patient cohort with MST…
RT @rsabouny: Second paper from ShuttLab @MitoMORPH this month! International collaboration comprising the largest patient cohort with MST…
RT @MitoMORPH: Two new papers from PhD Phenom Rasha @rsabouny in the ShuttLab @MitoMORPH, looking at mtDNA depletion when mitochondrial fus…
RT @MitoMORPH: Two new papers from PhD Phenom Rasha @rsabouny in the ShuttLab @MitoMORPH, looking at mtDNA depletion when mitochondrial fus…
RT @rsabouny: Second paper from ShuttLab @MitoMORPH this month! International collaboration comprising the largest patient cohort with MST…
RT @MitoMORPH: Two new papers from PhD Phenom Rasha @rsabouny in the ShuttLab @MitoMORPH, looking at mtDNA depletion when mitochondrial fus…
Second paper from ShuttLab @MitoMORPH this month! International collaboration comprising the largest patient cohort with MSTO1 mutations. We show that mutations in the mitochondrial fusion protein MSTO1 lead to mtDNA depletion & abnormal mtDNA nucleoi
Two new papers from PhD Phenom Rasha @rsabouny in the ShuttLab @MitoMORPH, looking at mtDNA depletion when mitochondrial fusion is impaired in mitochondrial disease: https://t.co/7ipniOHY2P https://t.co/Sl1Htii0xX /1
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. https://t.co/4BHQqk3eLx
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. https://t.co/gcT0HDnhK2