A NEW way in which hereditary human disease can strike has been found. A snippet of mitochondrial DNA can invade a cell’s nucleus, lodging itself in a gene vital to development. Leslie Biesecker of the National Human Genome Research Institute in Bethesda, Maryland, and his team found that this caused Pallister-Hall syndrome in one patient. They suspect that the mutation occurred in the father’s sperm or immediately after the patient was conceived in Ukraine, shortly after the Chernobyl accident (Human Genetics, vol 112, p 303). Radiation could have damaged the cell’s mitochondria.
To continue reading, today with our introductory offers
Advertisement
More from New Scientist
Explore the latest news, articles and features

Technology
US government wants to have a useful quantum computer by 2028
News

Life
Childbirth for many primate species is even harder than for humans
News

Humans
Humans sleep the least of all apes – is it the secret to our success?
Features

ÎçÒ¹¸£Àû1000¼¯ºÏ
Your menstrual cycle may affect how well vaccines work
News
Popular articles
Trending New Scientist articles
1
Humans sleep the least of all apes – is it the secret to our success?
2
Where, when and how to watch the 2026 solar eclipse
3
Remote-controlled cockroach swarm can now breathe underwater
4
US government wants to have a useful quantum computer by 2028
5
Our verdict on The Selfish Gene: An unpopular piece of popular science
6
Europe’s heatwave is the hottest and most humid ever
7
How some people's brains make an extraordinary recovery from stroke
8
We’ve uncovered a master gene that switches on human development
9
Fossil fruits show flowering plants flourished in time of dinosaurs
10
If you aren't terrified by this heatwave, you should be