US2014141439A1PendingUtilityA1
Methods and compositions for identifying increased risk of developing fragile x-associated disorders
Est. expiryOct 2, 2027(~1.2 yrs left)· nominal 20-yr term from priority
C12Q 1/6883C12Q 2600/154C12Q 2600/156C12Q 2600/158C12Q 2600/16
53
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Claims
Abstract
The present invention provides compositions and methods of identifying a subject as having an increased risk of developing fragile X-associated tremor and ataxia syndrome (FXTAS) or identifying a subject having an increased risk of developing fragile X syndrome (FXS), comprising analyzing messenger RNA (mRNA) transcripts and/or translation products of the antisense gene ASFMR1.
Claims
exact text as granted — not AI-modifiedThat which is claimed is:
1 - 37 . (canceled)
38 . A kit comprising one or more reagents for the detection of an ASFMR1e mRNA transcript comprising the nucleotide sequence of SEQ ID NO:5 or a nucleotide sequence that is at least 95% identical to the nucleotide sequence of SEQ ID NO:5.Join the waitlist — get patent alerts
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