Barriers to diagnosis of a rare neurological disorder in China - Lived experiences of Rett Syndrome families
Rett syndrome is a rare neurological disorder affecting girls and usually caused by a mutation on the MECP2 gene. It is estimated that approximately 1,000 girls are born every year in China with Rett syndrome but far fewer have received a diagnosis. Fourteen of 74 Chinese families known to the Inter...
| Main Authors: | , , , , |
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| Format: | Journal Article |
| Published: |
John Wiley & Sons, Inc.
2012
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| Subjects: | |
| Online Access: | http://hdl.handle.net/20.500.11937/26128 |