Birgit Weiß
Hat mitgewirkt an:
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Retinoic acid catabolizing enzyme CYP 26C1 is a genetic modifier in SHOX deficiency
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Identification of ZBTB26 as a novel risk factor for congenital hypothyroidism
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Identification of transient receptor potential channel 4-associated protein as a novel candidate gene causing congenital primary hypothyroidism
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Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation