KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation - Concepedia

Concepedia

Publication | Open Access

KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation

DOI Full Paper Access

85

Citations

18

References

2011

Year

Mustapha Amyere, Thomas Vogt, Joe J. Hoo, F Brandrup, Anette Bygum, Laurence M. Boon, Miikka Vikkula

Journal of Investigative Dermatology

Mendelian DisorderGenetic DisorderGeneticsMolecular GeneticsMedicine

References

	Year	Citations

Page 1