Back
  1. Home
  2. Profile of Joseph LACROIX (ULiège)
Profil

LACROIX Joseph

Département des Services Logistiques > Secteur manutention

See author's contact details
Main Referenced Co-authors
Debray, François-Guillaume  (1)
Decarie, J. C. (1)
Janvier, Annie (1)
Laframboise, R. (1)
Maranda, B. (1)
Main Referenced Disciplines
Genetics & genetic processes (1)

Publications (total 1)

The most downloaded
1 downloads
DEBRAY, F.-G., Morin, C., Janvier, A., Villeneuve, J., Maranda, B., Laframboise, R., LACROIX, J., Decarie, J. C., Robitaille, Y., Robinson, B. H., & Mitchell, G. A. (2011). LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency. Journal of Medical Genetics. doi:10.1136/jmg.2010.081976 https://hdl.handle.net/2268/87737

The most cited

81 citations (Scopus®)

DEBRAY, F.-G., Morin, C., Janvier, A., Villeneuve, J., Maranda, B., Laframboise, R., LACROIX, J., Decarie, J. C., Robitaille, Y., Robinson, B. H., & Mitchell, G. A. (2011). LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency. Journal of Medical Genetics. doi:10.1136/jmg.2010.081976 https://hdl.handle.net/2268/87737

DEBRAY, F.-G., Morin, C., Janvier, A., Villeneuve, J., Maranda, B., Laframboise, R., LACROIX, J., Decarie, J. C., Robitaille, Y., Robinson, B. H., & Mitchell, G. A. (2011). LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency. Journal of Medical Genetics. doi:10.1136/jmg.2010.081976
Peer Reviewed verified by ORBi

Contact ORBi