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muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a
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POMT1
Diversification of transcriptional modulation: Large-scale identification and characterization of putative alternative promoters of human genes
B3GNT1
Expression cloning of cDNA encoding a human ����-1,3-N-acetylglucosaminyltransferase that is essential for poly-N-acetyllactosamine synthesis
GMPPB
Towards a proteome-scale map of the human protein-protein interaction network.
POMT2
Murine and human SDF2L1 is an endoplasmic reticulum stress-inducible gene and encodes a new member of the Pmt/rt protein family
POMGNT1
Cloning and expression of a novel UDP-GlcNAc:alpha-D-mannoside beta1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I
FKTN
Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33
LARGE
The DNA sequence of human chromosome 22
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Amino sugar and nucleotide sugar metabolism
Homo sapiens (human)
one gene
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Cancer Gene Census
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