bibliographic entry 10201327 [be/10201327]
https://w3id.org/oc/corpus/be/10201327

is a

• bibliographic reference

content

• Bujakowska K. M. et al. Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome. Hum. Mol. Genet. 24, 230–242 (2015). PMID: 25168386

references

• https://w3id.org/oc/corpus/br/3670695