bibliographic entry 6738227 [be/6738227]
https://w3id.org/oc/corpus/be/6738227

is a

• bibliographic reference

content

• Halbritter J, Bizet AA, Schmidts M, Porath JD, Braun DA, Gee HY, McInerney‐Leo AM, Krug P, Filhol E, Davis EE, Airik R, Czarnecki PG, Lehman AM, Trnka P, Nitschké P, Bole‐Feysot C, Schueler M, Knebelmann B, Burtey S, Szabó AJ et al (2013) Defects in the IFT‐B component IFT172 Cause Jeune and Mainzer‐Saldino syndromes in humans. Am J Hum Genet 93: 915–925 PMID: 24140113

references

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