Aicardi-Goutières syndrome and dyschromatosis symmetrica hereditaria due to compound heterozygous mutation of ADAR1, presentation of two cases.
Ruben Linares-NavarroSonsoles Delgado-VicenteAquilina Jiménez-GonzálezVíctor Onecha-VallejoMaría Criado-OteroPublished in: International journal of dermatology (2023)
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