Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13
2007
Lesueur, F., Bouadjar, B., Lefevre, C., Jobard, F., Audebert, S., Lakhdar, H., Martin, L., Tadini, G., Karaduman, A., Emre, S., Saker, S., Lathrop, M. and Fischer, J.:
J Invest Dermatol 127 (2007) 829-34.
