About: Autosomal dominant optic atrophy with unilateral facial palsy: a new hereditary condition?

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/bmj/periodical/jmg/1999/volume_36/issue_3/w
Subject	Short Report Eye Diseases optic atrophy Hereditary eye disease unilateral facial palsy
Title	Autosomal dominant optic atrophy with unilateral facial palsy: a new hereditary condition?
has manifestation of work	http://hub.abes.fr/bmj/periodical/jmg/1999/volume_36/issue_3/B3598D6B5B2C7CBEE053120B220A90C5/m/web http://hub.abes.fr/bmj/periodical/jmg/1999/volume_36/issue_3/B3598D6B5B2C7CBEE053120B220A90C5/m/print
related by	http://hub.abes.fr/bmj/periodical/jmg/1999/volume_36/issue_3/B3598D6B5B2C7CBEE053120B220A90C5/authorship/1 http://hub.abes.fr/bmj/periodical/jmg/1999/volume_36/issue_3/B3598D6B5B2C7CBEE053120B220A90C5/authorship/2 http://hub.abes.fr/bmj/periodical/jmg/1999/volume_36/issue_3/B3598D6B5B2C7CBEE053120B220A90C5/authorship/3
Abstract	A mother and daughter are reported with bilateral optic atrophy with onset in infancy and unilateral facial palsy. This appears to be a novel autosomal dominant disorder.
article type	brief-report
publisher identifier	9811
is part of this journal	Journal of Medical Genetics
PubMed ID	10204856

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