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A prevalent mutation for galactosemia among black Americans.
Lai K, Langley SD, Singh RH, Dembure PP, Hjelm LN, Elsas LJ 2nd. Lai K, et al. J Pediatr. 1996 Jan;128(1):89-95. doi: 10.1016/s0022-3476(96)70432-8. J Pediatr. 1996. PMID: 8551426
Molecular basis for Duarte and Los Angeles variant galactosemia.
Langley SD, Lai K, Dembure PP, Hjelm LN, Elsas LJ. Langley SD, et al. Am J Hum Genet. 1997 Feb;60(2):366-72. Am J Hum Genet. 1997. PMID: 9012409 Free PMC article.
Black children deficient in galactose 1-phosphate uridyltransferase: correlation of activity and immunoreactive protein in erythrocytes and leukocytes.
Landt M, Ritter D, Lai K, Benke PJ, Elsas LJ, Steiner RD. Landt M, et al. J Pediatr. 1997 Jun;130(6):972-80. doi: 10.1016/s0022-3476(97)70286-5. J Pediatr. 1997. PMID: 9202622
The molecular biology of galactosemia.
Elsas LJ 2nd, Lai K. Elsas LJ 2nd, et al. Genet Med. 1998 Nov-Dec;1(1):40-8. doi: 10.1097/00125817-199811000-00009. Genet Med. 1998. PMID: 11261429 Review.
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