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Q36286534-DCD7F1ED-3994-46CC-BE9A-B1BE8803B263
Q36286534-DCD7F1ED-3994-46CC-BE9A-B1BE8803B263
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Statement
http://www.wikidata.org/entity/statement/Q36286534-DCD7F1ED-3994-46CC-BE9A-B1BE8803B263
MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
P2860
Q36286534-DCD7F1ED-3994-46CC-BE9A-B1BE8803B263
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36286534-DCD7F1ED-3994-46CC-BE9A-B1BE8803B263
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wasDerivedFrom
871453137557db385b8d8f8f5efe40b7f11112cb
P2860
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.