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You searched for: Author/Creator Wiesener, Antje

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1. Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking. (9th January 2020)

2. ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation. (June 2017)

4. Further characterization of Borjeson‐Forssman‐Lehmann syndrome in females due to de novo variants in PHF6. Issue 3 (14th June 2022)

5. Molecular diagnosis of kidney transplant failure based on urine. Issue 5 (20th January 2020)