Feng Y. et al. 1997

Feng Y., Absher D., Eberhart D.E., Brown V., Maker H.E., and Warren S.T., 1997. FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association. Mol Cell 1: 109-118.

Смотрите также:

Эпигенетика и синдром ломкой X-хромосомы

FMRP Белки