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- NP719319.RAZ0Qjgk6RCZm5LSX5cE3yCB0vX9yf6S4lvbAgQrVK5Rc130_assertion type Assertion NP719319.RAZ0Qjgk6RCZm5LSX5cE3yCB0vX9yf6S4lvbAgQrVK5Rc130_head.
- NP719319.RAZ0Qjgk6RCZm5LSX5cE3yCB0vX9yf6S4lvbAgQrVK5Rc130_assertion description "[Mutations in the CDKL5 gene have been associated with the early-onset seizure variant of Rett syndrome and mutations in FOXG1 have been associated with the congenital Rett syndrome variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719319.RAZ0Qjgk6RCZm5LSX5cE3yCB0vX9yf6S4lvbAgQrVK5Rc130_provenance.
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- NP719319.RAZ0Qjgk6RCZm5LSX5cE3yCB0vX9yf6S4lvbAgQrVK5Rc130_assertion SIO_000772 22968132 NP719319.RAZ0Qjgk6RCZm5LSX5cE3yCB0vX9yf6S4lvbAgQrVK5Rc130_provenance.
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