Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome. [electronic resource]
Producer: 20200303Description: 21 p. digitalISSN:- 1471-2350
- Adolescent
- Adult
- Bone Density -- genetics
- Bone Diseases -- diagnostic imaging
- Child
- Child, Preschool
- Female
- Fractures, Bone -- diagnostic imaging
- Humans
- Male
- Methyl-CpG-Binding Protein 2 -- genetics
- Mutation
- Osteoporosis -- diagnostic imaging
- Rett Syndrome -- diagnostic imaging
- Scoliosis -- diagnostic imaging
- Severity of Illness Index
- Young Adult
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Publication Type: Journal Article
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