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First Korean case of Emberger syndrome (primary lymphedema with myelodysplasia) with a novel GATA2 gene mutation
Sang-Kyung SEO; Kyu-Yeun KIM; Seo-Ae HAN; Joon-Seok YOON; Sang-Yong SHIN; Sang-Kyun SOHN; Joon-Ho MOON.
The Korean Journal of Internal Medicine ; : 188-190, 2016.
Article in En | WPRIM | ID: wpr-220485
Responsible library: WPRO
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Full text: 1 Index: WPRIM 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: En Journal: The Korean Journal of Internal Medicine Year: 2016 Type: Article
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Full text: 1 Index: WPRIM 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: En Journal: The Korean Journal of Internal Medicine Year: 2016 Type: Article