Author:
Trivedi Dhiraj J.,Haridas Vikram
Publisher
Springer Science and Business Media LLC
Reference13 articles.
1. Srsen S, Miller CR, Fregin A, Srsnova K. Alkaptonuria in slovakia: 32 year research on phenotype and genotype. Mol Genet Metab. 2002;75(4):353–9 (PMID- 12051967).
2. Srsen S, Zatková A, de Bernabe DB, Poláková H, et al. High frequency of alcaptonuria in slovakia: evidence for the appearance of multiple mutations in HGO involving different mutational hot spots. Am J Hum Genet. 2000;67(5):1333–9 (PMID-11017803).
3. Khadagawat R, Teckchandani R, Garg P, Arya A, Choudhary B. Alkaptonuria: early detection. Ind J Paediat. 1994;31:593–4.
4. Tarini GK, Ravindran V, Hema N. Alkaptonuria. Ind J Dermatol. 2011;56(2):194–6 (PMID-21716546).
5. Datta AK, Mandal S, Dasgupta A, Ghosh TK. Alkaptonuria diagnosed in a 4-month-old baby girl: a case report. Case J. 2008;1(1):308. doi: 10.1186/1757-1626-1-308 .
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