Arq. NeuroPsiquiatr. vol.71 número10

Cyst infection in hospital-admitted autosomal dominant polycystic kidney disease patients is predominantly multifocal and associated with kidney and liver

Although SNPs of this gene have been associated with human prion disease, no polymorphisms of the bovine CALHM1 gene, which shares 93% protein sequence identity with human CALHM1

In contrast, Dp260 lacks the cytokeratin filament–binding domain and portions of the synemin­ and actin­ binding domains, which likely alters the binding affinities to both

he autosomal dominant and de- myelinating type (CMT1) associated with duplication of the PMP22 gene (CMT1A) is the most prevalent subtype around the world, including Brazil 1 , and

ALS17 (MIM #614696) represents an autosomal dominant form of lower motor neuron dominant familial ALS (some- times associated with FTD) related to missense heterozy- gous mutations

258 Familial exudative vitreoretinopathy (FEVR) associated with infantile osteoporosis: case report.. Arq

Based on the cross-reactivity obtained using the polyclonal antisera, as well as the identification of a protein that was larger (~65 kDa) than predicted,

Lipoprotein glomerulopathy (LPG) is a rare autosomal recessive glomeru- lopathy associated with the deposition of lipoprotein thrombi in the capillary lumina due to apoE