Further delineation of DDX3X syndrome
Clin Dysmorphol
.
2019 Jul;28(3):151-153.
doi: 10.1097/MCD.0000000000000263.
Authors
Nicolas M Chanes
1
,
Joaquin Wong
2
,
Yves Lacassie
3
Affiliations
1
Louisiana State University, Baton Rouge.
2
Department of Neurology.
3
Department of Pediatrics, Division of Genetics, LSU Health Sciences Center and Children's Hospital, New Orleans, Louisiana, USA.
PMID:
30817323
DOI:
10.1097/MCD.0000000000000263
No abstract available
Publication types
Case Reports
MeSH terms
Child
DEAD-box RNA Helicases / genetics*
DEAD-box RNA Helicases / metabolism*
Female
Humans
Intellectual Disability / genetics
Mutation
Syndrome
Substances
DDX3X protein, human
DEAD-box RNA Helicases