×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Bardet-Biedl syndrome: Antenatal presentation of forty-five fetuses with biallelic pathogenic variants in known Bardet-Biedl syndrome genes.
30614526
2019
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy.
30718709
2019
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
Diagnostic exome sequencing in 266 Dutch patients with visual impairment.
28224992
2017
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Improving the management of Inherited Retinal Dystrophies by targeted sequencing of a population-specific gene panel.
27032803
2016
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Targeted multi-gene panel testing for the diagnosis of Bardet Biedl syndrome: Identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes.
26518167
2015
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
A paradigm shift in the delivery of services for diagnosis of inherited retinal disease.
22581970
2012
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
BBS1 mutations in a wide spectrum of phenotypes ranging from nonsyndromic retinitis pigmentosa to Bardet-Biedl syndrome.
23143442
2012
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
Genotype-phenotype correlations in Bardet-Biedl syndrome.
22410627
2012
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 gene.
22940089
2012
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
BBS1 mutations in a wide spectrum of phenotypes ranging from nonsyndromic retinitis pigmentosa to Bardet-Biedl syndrome.
23143442
2012
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary cilia.
21517826
2011
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genes.
21642631
2011
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
Bardet-Biedl syndrome: a study of the renal and cardiovascular phenotypes in a French cohort.
20876674
2011
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary cilia.
21517826
2011
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome.
20498079
2010
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease.
20177705
2010
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
A novel founder BBS1 mutation explains a unique high prevalence of Bardet-Biedl syndrome in the Faroe Islands.
18669544
2009
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Bardet-biedl syndrome: an atypical phenotype in brothers with a proven BBS1 mutation.
18766993
2008
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Retinal morphology in patients with BBS1 and BBS10 related Bardet-Biedl Syndrome evaluated by Fourier-domain optical coherence tomography.
17980398
2008
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity.
18032602
2007
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
Dissection of epistasis in oligogenic Bardet-Biedl syndrome.
16327777
2006
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
Testing for triallelism: analysis of six BBS genes in a Bardet-Biedl syndrome family cohort.
15770229
2005
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Testing for triallelism: analysis of six BBS genes in a Bardet-Biedl syndrome family cohort.
15770229
2005
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
CausalMutation
disease
CLINVAR
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome.
15314642
2004
×
Entrez Id:
254359
Gene Symbol:
ZDHHC24
ZDHHC24
0.100
GeneticVariation
disease
CLINVAR
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).
12524598
2003