Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: a case report
Abstract Background Cyanosis is usually associated with serious conditions requiring urgent treatment in the neonatal intensive care unit (NICU). Hemoglobin M (Hb M) disease is one type of congenital methemoglobinemia characterized by cyanosis. Among these variants, α-globin chain mutations such as...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
BMC,
2019-07-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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