The gene for Best's macular dystrophy is located at 11q13 in a Swedish family

scientific article (publication date: September 1992)

The gene for Best's macular dystrophy is located at 11q13 in a Swedish family is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/J.1399-0004.1992.TB03229.X
P698PubMed publication ID1395087

P50authorCaroline GraffQ37374962
P2093author name stringG Holmgren
K Johansson
C Wadelius
E Lundgren
K H Gustavson
K Forsman
S Nordström
E Westermark
P2860cites workVitelliform Macular DegenerationQ54074270
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectSwedenQ34
P304page(s)156-9
P577publication date1992-09-01
P1433published inClinical GeneticsQ5133760
P1476titleThe gene for Best's macular dystrophy is located at 11q13 in a Swedish family
P478volume42

Reverse relations

cites work (P2860)
Q24628598A 3-Mb contig from D11S987 to MLK3, a gene-rich region in 11q13
Q24628148A gene map of the Best's vitelliform macular dystrophy region in chromosome 11q12-q13.1
Q43146321A novel locus on 19q13 associated with autosomal-dominant macular dystrophy in a large Greek family
Q34346415Atypical vitelliform macular dystrophy misdiagnosed as chronic central serous chorioretinopathy: case reports
Q38170399Bestrophin 1--Phenotypes and Functional Aspects in Bestrophinopathies
Q50556554Confirmation of linkage to 1q21-31 in a Danish autosomal dominant juvenile-onset glaucoma family and evidence of genetic heterogeneity.
Q34272304Confronting complexity: the interlink of phototransduction and retinoid metabolism in the vertebrate retina
Q33682728Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy
Q40937286Genetic and molecular studies of macular dystrophies: recent developments
Q35889816High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11.
Q41652312Identification of genes causing photoreceptor degenerations leading to blindness
Q24315031Identification of the gene responsible for Best macular dystrophy
Q34348965Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity
Q71739592Mapping eight new polymorphisms in 11q13 in the vicinity of multiple endocrine neoplasia type 1: identification of a new distal recombinant
Q42071308Molecular evidence for non-penetrance in Best's disease.
Q37324803Molecular genetics of macular dystrophies
Q46394220Mutation analysis of the VMD2 gene in thai families with best macular dystrophy
Q37746102Nanoparticles for retinal gene therapy
Q40663589North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q16.2.
Q60064503Peripherin and the vision thing
Q35888865Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1.
Q41930072Still no evidence for heterogeneity in Best's vitelliform macular dystrophy
Q35213761The genetics of inherited macular dystrophies
Q22253395VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies

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