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NMR-based urinalysis for beta-ketothiolase deficiency.
Law CY, Lam CW, Ching CK, Yau KC, Ho TW, Lai CK, Mak CM. Law CY, et al. Among authors: mak cm. Clin Chim Acta. 2015 Jan 1;438:222-5. doi: 10.1016/j.cca.2014.08.041. Epub 2014 Sep 4. Clin Chim Acta. 2015. PMID: 25195009
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: identification of 17 novel mutations and its genetic heterogeneity.
Mak CM, Lam CW, Tam S, Lai CL, Chan LY, Fan ST, Lau YL, Lai JY, Yuen P, Hui J, Fu CC, Wong KS, Mak WL, Tze K, Tong SF, Lau A, Leung N, Hui A, Cheung KM, Ko CH, Chan YK, Ma O, Chau TN, Chiu A, Chan YW. Mak CM, et al. Among authors: mak wl. J Hum Genet. 2008;53(1):55-63. doi: 10.1007/s10038-007-0218-2. Epub 2007 Nov 22. J Hum Genet. 2008. PMID: 18034201
Hereditary spastic paraplegias.
Lau KK, Ching CK, Mak CM, Chan YW. Lau KK, et al. Among authors: mak cm. Hong Kong Med J. 2009 Jun;15(3):217-20. Hong Kong Med J. 2009. PMID: 19494379 Free article.
127 results