bibliographic entry 10201322 [be/10201322]
https://w3id.org/oc/corpus/be/10201322

is a

• bibliographic reference

content

• Halbritter J. et al. Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans. Am. J. Hum. Genet. 93, 915–925 (2013). PMID: 24140113

references

• https://w3id.org/oc/corpus/br/3349205