Isolated and contiguous glycerol kinase gene disorders: A review
Author:
Affiliation:
1. ; Department of Pediatrics/Metabolic Diseases; University Medical Center Utrecht; Utrecht The Netherlands
2. ; Department of Medical Genetics; University Medical Center Utrecht; Utrecht The Netherlands
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005660826652/fullpdf
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3. Patient with an Xp21 con-tiguous gene deletion syndrome in association with agenesis of the corpus callosum;Baranzini;Am J Med Genet,1997
4. Absence of brain Dp140 isoform and cognitive impairment in Becker muscular dystrophy;Bardoni;Lancet,1999
5. The concordance of X-linked glycerol kinase de¢ciency with X-linked adrenal hypoplasia in two families;Bartley;Lancet,1982
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