Product cited in:
Westphal, Xiao, Kwok et al.: "Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic." in: Human mutation, Vol. 22, Issue 5, pp. 420-1, 2003 (PubMed).
Ota, Suzuki, Nishikawa et al.: "Complete sequencing and characterization of 21,243 full-length human cDNAs." in: Nature genetics, Vol. 36, Issue 1, pp. 40-5, 2003 (PubMed).
Gerhard, Wagner, Feingold et al.: "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." in: Genome research, Vol. 14, Issue 10B, pp. 2121-7, 2004 (PubMed).
Eklund, Sun, Yang et al.: "Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation." in: Biochemical and biophysical research communications, Vol. 339, Issue 3, pp. 755-60, 2005 (PubMed).
Gregory, Barlow, McLay et al.: "The DNA sequence and biological annotation of human chromosome 1." in: Nature, Vol. 441, Issue 7091, pp. 315-21, 2006 (PubMed).