OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin - Concepedia

Concepedia

Publication | Open Access

OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin

DOI Full Paper Access

207

Citations

51

References

2009

Year

Karlien L. M. Coene, Ronald Roepman, Dan Doherty, Bushra Afroze, Hester Y. Kroes, Stef J.F. Letteboer, Lock Hock Ngu, Bartłomiej Budny, Erwin van Wijk, Nicholas T. Gorden,

The American Journal of Human Genetics

X-linked Joubert SyndromeMendelian DisorderGenetic DisorderGeneticsPathogenesisOfd1 IsFragile X SpectrumPathologyMolecular GeneticsLca5-encoded LebercilinDisease Gene IdentificationMedicine

References

	Year	Citations

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