Πλοήγηση ανά Θέμα "autosomal dominant inheritance"
Αποτελέσματα 1-3 από 3
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Clinical immunology quiz-Case 6
(2009) -
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration
(2014)Neurodegenerative diseases affecting the macula constitute amajor cause of incurable vision loss and exhibit considerable clinical and genetic heterogeneity, from early-onset monogenic disease to multifactorial lateonset ... -
Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13
(2008)Five loci for restless legs syndrome (RLS) on chromosomes 12q, 14q, 9p, 2q, and 20p (RLS1-RLS5) have been mapped in RLS families, with a recessive in the first and autosomal-dominant mode of inheritance in the latter cases. ...