bibliographic entry 10201362 [be/10201362]
https://w3id.org/oc/corpus/be/10201362

is a

• bibliographic reference

content

• Tammachote R. et al. Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3. Hum. Mol. Genet. 18, 3311–3323 (2009). PMID: 19515853

references

• https://w3id.org/oc/corpus/br/3068512