Fragile X-associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene
DZ Loesch, S Sherwell, G Kinsella, F Tassone, A Taylor, D Amor, S Sung, A Evans
Clinical Genetics | WILEY | Published : 2012
Awarded by National Institutes of Child Health and Human Development
Awarded by NHMRC
Awarded by National Institute of Health
This study was supported by the National Institutes of Child Health and Human Development Grant HD 36071 and the NHMRC project grant no 330400 to Dr D. Z. L., and by the National Institute of Health grant HD02274 to Dr F. T. We wish to express special thanks to the family of the individual presented here for their cooperation.