bibliographic entry 8304318 [be/8304318]
https://w3id.org/oc/corpus/be/8304318

is a

• bibliographic reference

content

• Meyer, E, Lim, D, Pasha, S, Tee, LJ, Rahman, F, Yates, JR. Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome), PLoS Genet, 2009, 5, e1000423, PMID: 19300480

references

• https://w3id.org/oc/corpus/br/4845088