It is noteworthy that SSCP has already enjoyed an enormous success in unknown mutation screening and it is still the method of choice in many molecular genetic laboratories.
SSCP did its prove, but nowadays a more powerful technique is widely employed, NGS that will provide you all variants and all sorts of variants along the genome you're studying. And now it is so powerful and reliable that it's used in disease founding ans diagnosis.
see this paper took from thousands in pubmed (Article Panel-based next generation sequencing as a reliable and eff...