Min Ae Lee-Kirsch

Ärztin, Kinderärztin

Works:

Molekulargenetische Analyse multifaktorieller Krankheiten
Phenotypic Variability in a Family with Aicardi-Goutières Syndrome Due to the Common A177T RNASEH2B Mutation
Decoding TREX2 : Molecular and cellular characterisation of a 3'-5' DNA exonuclease
Familial Chilblain Lupus – A Monogenic Form of Cutaneous Lupus Erythematosus due to a Heterozygous Mutation in TREX1

All Objects (21)

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Min Ae Lee-Kirsch

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