First Korean case of Emberger syndrome (primary lymphedema with myelodysplasia) with a novel GATA2 gene mutation
The Korean Journal of Internal Medicine
;
: 188-190, 2016.
Article
in English
| WPRIM
| ID: wpr-220485
ABSTRACT
No abstract available.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Phenotype
/
Myelodysplastic Syndromes
/
DNA Mutational Analysis
/
Frameshift Mutation
/
Genetic Predisposition to Disease
/
GATA2 Transcription Factor
/
Republic of Korea
/
Hearing Loss, Sensorineural
/
Lymphedema
Limits:
Female
/
Humans
Country/Region as subject:
Asia
Language:
English
Journal:
The Korean Journal of Internal Medicine
Year:
2016
Type:
Article
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