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ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
Known as:
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATION
, Mecp2-Related Severe Neonatal Encephalopathy
National Institutes of Health
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9 relations
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Broader (1)
Mental Retardation, X-Linked
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Спектр вариаций числа копий гена MeCP2 в Российской когорте детей с нарушением интеллекта, врожденными пороками развития, эпилепсией и аутизмом
С Б Ворсанова
,
Ю. Б. Юров
,
+5 authors
И. Ю. Юров
2016
Corpus ID: 132818076
2014
2014
Zespół duplikacji MECP2 – opis przypadku
Ewa Jamroz
,
Ewa Grzywna-Rożenek
,
Antoni Pyrkosz
2014
Corpus ID: 72220989
2014
2014
Triheptanoin diet improves insulin sensitivity in Mecp2 KO mice.
J. Min
,
A. Susan
,
+5 authors
V. Gabriele
2014
Corpus ID: 87555947
2014
2014
Chow-fed Mecp2 KO mice have significantly increased WAT mass and serum leptin, and decreased rotarod performance.
J. Min
,
A. Susan
,
+5 authors
V. Gabriele
2014
Corpus ID: 74535365
2014
2014
Anaplerotic triheptanoin diet normalizes steady-state betahydroxybutyrate (BHBA) in liver and muscle of Mecp2 KO mice.
J. Min
,
A. Susan
,
+5 authors
V. Gabriele
2014
Corpus ID: 86250014
2002
2002
MECP2 유전자의 돌연변이 유형과 X 염색체 불활성화가 Rett 증후군의 표현형에 미치는 영향
채종희
2002
Corpus ID: 83108397
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