Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome.

Caffarelli, Carla

Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome. [electronic resource] - BMC medical genetics 01 2020 - 21 p. digital

Publication Type: Journal Article

1471-2350

10.1186/s12881-020-0960-2 doi


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