Bone Mass in Rett Syndrome: Association with Clinical Parameters and MECP2 Mutations

Rett Syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutations in the MECP2 gene. In 49 female RTT children, ages 1.9–17 years, bone mass was assessed and correlated with clinical parameters and mutations involving the MECP2 gene. We also studied 5 adult females, ages 20–33 years...

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Main Authors: Shapiro, Jay R., Bibat, Genila, Hiremath, Girish, Blue, Mary E., Hundalini, Shilpa, Yablonski, Theodore, Kantipuly, Aditi, Rohde, Charles, Johnston, Michael, Naidu, SakkuBai
Format: Artigo
Jezik:Inglês
Izdano: 2010
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Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3074246/
https://ncbi.nlm.nih.gov/pubmed/20661168
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1203/PDR.0b013e3181f2edd2
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