Novel Mutations in ALOX12B in Patients with Autosomal Recessive Congenital Ichthyosis and Evidence for Genetic Heterogeneity on Chromosome 17p13 - Concepedia

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Novel Mutations in ALOX12B in Patients with Autosomal Recessive Congenital Ichthyosis and Evidence for Genetic Heterogeneity on Chromosome 17p13

DOI Full Paper Access

45

Citations

15

References

2006

Year

Fabienne Lesueur, B. Bouadjar, Caroline Lefèvre, Florence Jobard, Stéphanie Audebert, Hakima Lakhdar, Ludovic Martin, Gianluca Tadini, Ayşen Karaduman, Serap Emre,

Journal of Investigative Dermatology

Mendelian DisorderGenetic DisorderGeneticsChromosome 17P13Novel MutationsPathologyGenetic HeterogeneityMedicine

References

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