Journal article

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

Grants

Awarded by National Institutes of Child Health and Human Development


Awarded by NHMRC


Awarded by National Institute of Health


Funding Acknowledgements

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.