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Dive into the research topics where Loi Mo FUNG is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Inherited metabolic diseases in the Southern Chinese population: Spectrum of diseases and estimated incidence from recurrent mutations
Hui, J., Tang, N. L. S., Li, C. K., Law, L. K., To, K. F., Yau, P., Fung, S. L. M., Chong, J. S. C., Tsung, L., Chiang, G., Fung, E., Cheung, K. L., Yeung, W. L. & Fok, T. F., Aug 2014, In: Pathology. 46, 5, p. 375-382 8 p.Research output: Contribution to journal › Article › peer-review
29 Citations (Scopus) -
Functional interaction between SNPS and microsatellite in the transcriptional regulation of insulin-like growth factor 1
Chen, H. Y., Huang, W., Leung, V. H. K., Fung, S. L. M., Ma, S. L., Jiang, H. & Tang, N. L. S., Sept 2013, In: Human mutation. 34, 9, p. 1289-1297 9 p.Research output: Contribution to journal › Article › peer-review
Open Access22 Citations (Scopus) -
The first reported HLCS gene mutation causing holocarboxylase synthetase deficiency in a Vietnamese patient
Hui, J., Law, E., Chung, C., Fung, S., Yuen, P. & Tang, N., Aug 2012, In: World Journal of Pediatrics. 8, 3, p. 278-280 3 p.Research output: Contribution to journal › Article › peer-review
3 Citations (Scopus) -
CBS gene mutations found in a Chinese pyridoxine-responsive homocystinuria patient
Kwok, J. S. S., Fung, S. L. M., Lui, G. C. Y., Law, E. L. K., Chan, M. H. M., Leung, C. B. & Tang, N. L. S., Jan 2011, In: Pathology. 43, 1, p. 81-83 3 p.Research output: Contribution to journal › Letter › peer-review
6 Citations (Scopus) -
Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
Law, L. K., Tang, N. L. S., Hui, J., Fung, S. L. M., Ruiter, J., Wanders, R. J. A., Fok, T. F. & Lam, C. W. K., 27 Jun 2009, In: Clinica Chimica Acta. 404, 2, p. 95-99 5 p.Research output: Contribution to journal › Article › peer-review
50 Citations (Scopus)