4.8 Article

Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients

Related references

Note: Only part of the references are listed.
Review Biochemistry & Molecular Biology

FMR1: A gene with three faces

Ben A. Oostra et al.

BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (2009)

Article Genetics & Heredity

CGG repeat length correlates with age of onset of motor signs of the fragile X-associated tremor/ataxia syndrome (FXTAS)

Flora Tassone et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2007)