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2. A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators. Issue 3 (25th December 2018)

5. Genome‐wide association study identifies TNFSF15 associated with childhood asthma. Issue 1 (14th June 2021)

6. IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype. Issue 10 (14th August 2015)

7. Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies. Issue 3 (16th December 2015)

8. Microbiome analysis reveals that Ralstonia is responsible for decreased renal function in patients with ulcerative colitis. Issue 3 (4th March 2021)

9. OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin. Issue 11 (2nd November 2022)

10. Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in children. Issue 3 (21st March 2018)