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Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis-ichthyosis-deafness (KIDAR) syndrome.

Julia VornwegS GläserM Ahmad-AnwarAndreas David ZimmerM KuhnS HörerG C KorenkeJ GrothausH OttJudith Fischer
Published in: The British journal of dermatology (2021)
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