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pro vyhledávání: '"Theodore Yablonski"'
Autor:
Girish Hiremath, Aditi Kantipuly, Shilpa Hundalani, Jay R. Shapiro, Sakkubai Naidu, Charles A. Rohde, Theodore Yablonski, Genila Bibat, Michael V. Johnston, Mary E. Blue
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 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f659335d4b92d455a197ad3d4a636cbf
https://europepmc.org/articles/PMC3074246/
https://europepmc.org/articles/PMC3074246/
