Xp21.2 contiguous gene syndrome due to deletion involving glycerol kinase and Duchenne muscular dystrophy loci
Neurol India
.
2010 Jul-Aug;58(4):670-1.
doi: 10.4103/0028-3886.68690.
Authors
Ewa Jamroz
,
Justyna Paprocka
,
Ewa Popowska
,
Justyna Pytel
,
Elzbieta Ciara
,
Maciej Adamowicz
PMID:
20739824
DOI:
10.4103/0028-3886.68690
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child, Preschool
Cognition Disorders / etiology
Glycerol Kinase / genetics*
Humans
Male
Muscular Dystrophy, Duchenne / complications
Muscular Dystrophy, Duchenne / genetics*
Sequence Deletion / genetics*
Substances
Glycerol Kinase