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Q41934849-67C3333E-1A75-4EEF-B86E-58C7382B765E
Q41934849-67C3333E-1A75-4EEF-B86E-58C7382B765E
BestRank
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http://www.wikidata.org/entity/statement/Q41934849-67C3333E-1A75-4EEF-B86E-58C7382B765E
Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutation.
P2860
Q41934849-67C3333E-1A75-4EEF-B86E-58C7382B765E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41934849-67C3333E-1A75-4EEF-B86E-58C7382B765E
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type
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Statement
wasDerivedFrom
0c6058da6f2e19547f2aabc3c9df3687401eca0c
P2860
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.