Mahairas, G. et al., “Sequence-Tagged Connectors: A Sequence Approach to Mapping and Scanning the Human Genome,” Proceedings of the National Academy of Sciences of the United States of America, 96(17) :9739-9744. |
Mahairas et al., HS_5333_B1_GO6_SP6E RPCI-11 Human Male BAC Library Homo sapiens genomic clone Plate+909 Col-11 Row=N, genomic survey sequence, EMBL Database [online], 1999 [retrieved on Apr. 25, 2001]. Retrieved from the Internet <URL:http://srs.ebi.ac.uk/srs6bin/cgi-bin/wgetz?—id+b9841Gitof+−e+ [EMBL: ‘AQ673121’]> Accession No. AQ673121. |
Hagström-Toft, E. et al., “Lipolytic response during spontaneous hypoglycaemia in insulin-dependent diabetic subjects,” Hormone and Metabolic Research 30(9) :586-593 (1998). |
Sargent, C.A. et al., “Five cases of isolated glycerol kinase deficiency including two families: Failure to find genotype:phenotype correlation,” Journal of Medical Genetics 37 (6) :434-441 (2000). |
Sargent, C.A., Homo sapiens partial GK gene for glycerol kinase, exon 12 (glycerol kinase deficiency case), EMBL Database [Online], 1999 [retrieved on Apr. 25, 2001]. Retrieved from the Internet <URL:http://srs.ebi.ac.uk/srs6bin/cgi-bin/wgetz?-id+b9841Gitof+−e+ [EMBL: ‘AQ673121’]> Accession No. HSA252563/AJ252563. |
Schoonderwoerd K. et al., “Enhanced Lipolysis of Myocardial Triglycerides During Low-flow Ischemia and Anoxia in the Isolated Rat Heart,” Basic Research in Cardiology 84(2):165-173 (1989). |
Uhal, B.D. and Longmore, W.J., “Altered Glycerol Metabolism in the Type II Pneumocyte Isolated from Stretozotocin-Diabetic and BB Wistar Spontaneously Diabetic Rats, ” Federation Proceedings 44 (5) :1606 (1985). Abstract 6992. |
Gaudet, et al., “Glycerol as a Correlate of Impaired Glucose Tolerance: Dissection of a Complex System by Use of a Simple Genetic Trait”, Am. J. Hum. Genet. 66: 1558-1568 (2000). |
Sargent, et al., “H. sapiens glycerol kinase gene deficiency locus”, GenBank Accession No. X78211 (1994). |
Pelkonen, et al., “Metabolism of Glycerol on Diabetes Mellitus”, Diabetologia 3(1): 1-8 (1967). |
Rose and Haines, “Familial Hyperglycerolemia”, J. Clin. Invest. 61: 163-170 (1978). |
Pettigrew, et al., “Conserved Active Site Aspartates and Domain-Domain Interactions in Regulatory Properties of the Sugar Kinase Superfamily”, Archives of Biochemistry and Biophysics 349(2): 236-245 (1998). |
Sjarif, et al., “Clinical heterogeneity and noverl mutations in the glycerol kinase gene in three families with isolated glycerol kinase deficiency”, J. Med. Genet. 35(8) : 650-656 (1998). |
Walker, et al., “Mutations and Phenotype in Isolated Glycerol Kinase Deficiency”, Am. J. Hum. Genet. 58: 1205-1211 (1996). |
Blomquist, et al., “Glycerol kinase deficiency in two brothers with and without clinical manifestations”, Clin. Genet. 50: 375-379 (1996). |