MTRR gene variants may predispose to the risk of Congenital Heart Disease in Down syndrome patients of Indian origin
Egyptian Journal of Medical Human Genetics [The]. 2017; 18 (1): 61-66
in English
| IMEMR
| ID: emr-189218
ABSTRACT
Background:
Down syndrome [DS], also called as trisomy 21, is one of the most leading cause of intellectual disability. DS is associated with a number of phenotypes including Congenital Heart Disease [CHD], Leukemia, Alzheimer's disease, Hirschsprung's disease and others. DS affects about 1 in 700 live births
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Polymorphism, Genetic
/
Polymorphism, Restriction Fragment Length
/
Polymerase Chain Reaction
/
Risk
/
Ferredoxin-NADP Reductase
/
Genotype
/
Heart Defects, Congenital
Limits:
Humans
Language:
English
Journal:
Egypt. J. Med. Hum. Genet.
Year:
2017
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