DNA¹ analysis has revealed the identity of the "cursed blood" disorder² that afflicted³ the British Royal Family in the 19th and early 20th centuries.

DNA检测显示了19世纪以及20实际初期使英国皇室苦恼的“被诅咒的血统”的原因。

mutation⁴ was transmitted from Russian Empress Alexandra to her son Crown Prince Alexei" width="466" border="0" src="/upimg/091009/4_054728_1.jpg" />
The mutation was transmitted from Russian Empress Alexandra to her son Crown Prince Alexei

Scientists say the disease inherited（遗传，继承） by Queen Victoria's descendants was probably a severe form of the blood clotting⁶ disorder haemophilia B.

The scientists examined DNA samples extracted from the skeletal remains⁷（骨骼残骇） of Russia's Romanov family.

The research is published in the journal Science.

Their analysis included the remains of Queen Victoria's great grandson Crown Prince Alexei.

Scientists already knew that males of the Royal Family at that time suffered from a type of haemophilia（血友病）.

But their latest analysis of the remains of Victoria's Russian descendants helped identify the exact form.

Modern analytical⁸ techniques allowed the scientists to amplify⁹（扩大，详述） the very degraded DNA.

They discovered a mutation in a gene¹⁰ on the X chromosome¹¹ that codes for the production of Factor IX, a substance that causes blood to clot⁵.

This genetic¹² mutation is the cause of haemophilia B.

Because this blood disorder is linked to the X chromosome it passed on through the maternal¹³ line, but is only manifested（显示，出现） in male descendants.

This is because males have only one X chromosome, so the mutation on that single chromosome is "expressed" as the disease.

Females only carry the disease, because their second X chromosome is extremely unlikely to have this same, very rare mutation.

Dr Evgeny Rogaev from the University of Massachusetts led the research.

He told the BBC that it was the "final chapter" in the confirmation¹⁴ of the Romanov family's remains.

He added: "We have resolved（决定，解决） a medical mystery from the past."