- A Case of Xp21 Contiguous Gene Deletion Syndrome with Hyperglycerolemia, Congenital Adrenal Hypoplasia and Duchenne Muscular Dystrophy
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Shin DW, Huh J, Lee HJ, Park WI, Lee KJ, Shin YS, Sjarif DR, Poll-The B
- KMID: 1605945
- J Korean Pediatr Soc.
- 2001 Jan;44(1):83-88.
On Xp21 region several genes such as adrenal hypoplasia congenita(AHC) gene, glycerol kinase (GK) gene and Duchenne muscular dystrophy(DMD) gene are located contiguously. If there is a long deletion in... -
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