Neonatal Hyperbilirubinemia in infants with <it>G6PD c.563C > T</it><it>Variant</it>
<p>Abstract</p> <p>Background</p> <p>There is a strong correlation between glucose-6-phosphate dehydrogenase (G6PD) deficiency and neonatal hyperbilirubinemia with a rare but potential threat of devastating acute bilirubin encephalopathy. G6PD deficiency was observed in...
Saved in:
Main Authors: | Moiz Bushra (Author), Nasir Amna (Author), Khan Sarosh (Author), Kherani Salima (Author), Qadir Maqbool (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2012-08-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
G-6PD Screening in Neonatal Hyperbilirubinemia
by: Suvitha Thilakarajan, et al.
Published: (2015) -
G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population
by: Dewi A. Wisnumurti, et al.
Published: (2019) -
SLCO1B1 c.388A > G variant incidence and the severity of hyperbilirubinemia in Indonesian neonates
by: Radhian Amandito, et al.
Published: (2019) -
Identification of a novel SDHB c.563 T > C mutation responsible for Paraganglioma syndrome and genetic analysis of the SDHB gene in China: a case report
by: Heye Chen, et al.
Published: (2020) -
"Regenerating" Iα Gene Variants g. -385T>C and g. -243T>G in Type 2 Diabetes
by: Sadaf Saleem Uppal, et al.
Published: (2024)