Corrigendum: identi fi cation of the fi rst congenital ichthyosis case caused by a homozygous deletion in the alox12b gene due to chromosome 17 mixed uniparental disomy

HIGHLIGHTS

• who: Correction and collaborators from the Auxological Institute (IRCCS), ItalyTongji Medical College, Huazhong University of Science and Technology, Wuhan, China, Dermatology have published the article: Corrigendum: Identi fi cation of the fi rst congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy, in the Journal: (JOURNAL)

SUMMARY

ARCI, ALOX12B, whole-exome sequencing, mixed UPD (mixUPD), microtia A Corrigendum on Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy by . . .

 



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