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Whole exome sequencing detects CHST3 mutation in patient with acute promyelocytic leukemia: A case report

RATIONALE: Acute promyelocytic leukemia (APL) is a kind of acute myeloid leukemia, which was characterized by the presence of PML/RARα fusion gene. Mutations in CHST3 have been previously reported to be associated with a rare phenotype of skeleton dysplasia, known as Spondyloepiphyseal dysplasia. He...

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Detalles Bibliográficos
Autores principales:	Feng, Lili, Li, Ying, Jiang, Yujie, Wang, Na, Yuan, Dai, Fan, Juan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2018
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133617/ https://www.ncbi.nlm.nih.gov/pubmed/30200136 http://dx.doi.org/10.1097/MD.0000000000012214

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