Subclinical phenotypic expressions in heterozygous females of X-linked recessive bulbospinal neuronopathy
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference22 articles.
1. A family with adult spinal and bulbar muscular atrophy, X-linked inheritance and associated testicular failure;Arbizu;J. Neurol. Sci.,1983
2. Characterization of a murine gene expressed from the inactive X chromosome;Borsani;Nature,1991
3. A gene from the region of the human X inactivation centre is expressed exclusively from the inactivate X chromosome;Brawn;Nature,1991
4. Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome;Brockdorff;Nature,1991
5. Severity of X-linked recessive bulbospinal neuronopathy correlates with size of the tandem CAG repeat in androgen receptor gene;Doyu;Ann. Neurol.,1992
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