FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association (Q28115097)

3 January 2017

title

FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association (English)

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FMRP translational regulator 1

3 January 2017

main subject

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GOA release 2020-03-11

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Y. Feng

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3 January 2017

D. Absher

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3 January 2017

D. E. Eberhart

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3 January 2017

V. Brown

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3 January 2017

H. E. Malter

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3 January 2017

S. T. Warren

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3 January 2017

language of work or name

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1 December 1997

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3 January 2017

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3 January 2017

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3 January 2017

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3 January 2017

page(s)

109–118

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FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding

3 January 2017

cites work

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7 January 2021

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7 January 2021

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7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

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