Clinical utility gene card for: fragile X mental retardation syndrome, fragile X-associated tremor/ataxia syndrome and fragile X-associated primary ovarian insufficiency.
- Jacquemont S Service de génétique Médicale, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
- Birnbaum S
- Redler S
- Steinbach P
- Biancalana V
- 2011-05-05
Published in:
- European journal of human genetics : EJHG. - 2011
Ataxia
Female
Fragile X Mental Retardation Protein
Fragile X Syndrome
Humans
Male
Primary Ovarian Insufficiency
Sensitivity and Specificity
Syndrome
Tremor
Trinucleotide Repeats
- Language
-
- English
- Open access status
- bronze
- Identifiers
-
- DOI 10.1038/ejhg.2011.55
- PMID 21540884
- Persistent URL
- https://sonar.ch/global/documents/257141
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