Nucleic acid is the main material for storing, copying, and transmitting genetic information.
Gene sequencing is of great significance in DNA damage research, gene therapy, mutation …

Single-nucleotide polymorphisms (SNPs) are the simplest and most common type of DNA
variations in the human genome. This class of attractive genetic markers, along with point …

Sudden infant death syndrome (SIDS) is described as the sudden and unexplained death of
an apparently healthy infant younger than one year of age. Genetic studies indicate that up …

Background: Sudden infant death syndrome (SIDS) is a leading cause of postneonatal
mortality. Genetic heart diseases (GHDs) underlie some cases of SIDS. Objectives: This …

Background Sudden unexplained death may be the first manifestation of an unknown
inherited cardiac disease. Current genetic technologies may enable the unraveling of an …

In the forensic medicine field, molecular autopsy is the post-mortem genetic analysis
performed to attempt to unravel the cause of decease in cases remaining unexplained after …

Purpose This study aimed to evaluate genetic contributions to sudden unexpected death in
pediatrics (SUDP). Methods We phenotyped and performed exome sequencing for 352 …

In forensic medicine, one-third of the sudden deaths remain unexplained after medico-legal
autopsy. A major proportion of these sudden unexplained deaths (SUD) are considered to …

Importance Sudden infant death syndrome (SIDS) remains a leading cause of death during
the first year of life. The etiology of SIDS is complex and remains largely unknown. Objective …

Nemaline myopathy (NM) is a common form of congenital nondystrophic skeletal muscle
disease characterized by muscular weakness of proximal dominance, hypotonia, and …