Parkinson’s disease is a brain disorder that may be caused by mutations in several genes that code for the production of alpha-synuclein. Individuals who have Parkinson’s disease exhibit symptoms such as uncontrollable tremors, difficulty walking, and loss of coordination. How might geneticists determine where the mutations that cause Parkinson’s disease are located? PCR analysis gene mapping DNA fingerprinting STR analysis

They could use SNPs(Single nucleotide polymorphisms) of DNA, which are an anaylysis of chromosomes using high tech laser magnification. This SNPing allows scientist to more closely view specific genes in chromosomes that cause certain traits. It allows for a greater genetic mapping and could also be used to see mutations, if you know which chromosome to look at.

IDK, just an idea, SNPs were used to look at different species trait exhibition, I thought it might work for this if used properly.

the right answer is a. skin cells forming from sunlight.

the liver is an organ endowed with a fantastic ability to regenerate

. thus, if a hepatectomy (ablation) of 70% of the hepatic mass is performed in the rat, there is complete recovery in 7 to 10 days.

prokaryotes are beings that have existed since the existence of life on earth, and do not come from another realm.

ribosomes are organelles that exist naturally in eukaryotes, either in free form or attached to the endoplasmic reticulum.

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mark brainliest and have a great day!

one centimetre is equal to 0.01 metres