bibliographic entry 8003917 [be/8003917]
https://w3id.org/oc/corpus/be/8003917

is a

• bibliographic reference

content

• Mobley BC, Enns GM, Wong L-J, Vogel H (2009) A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy. Clin Neuropathol 28: 143–149. PMID: 19353847

references

• https://w3id.org/oc/corpus/br/6202030