×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Cystic cerebellar dysplasia and biallelic LAMA1 mutations: a lamininopathy associated with tics, obsessive compulsive traits and myopia due to cell adhesion and migration defects.
27095636
2016
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophy.
25105227
2014
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Ataxia, intellectual disability, and ocular apraxia with cerebellar cysts: a new disease?
24013853
2014
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
The laminin family.
23263632
2013
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Update on activities at the Universal Protein Resource (UniProt) in 2013.
23161681
2013
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
21937992
2011
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Mutations in Lama1 disrupt retinal vascular development and inner limiting membrane formation.
20048158
2010
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
The NCBI BioSystems database.
19854944
2010
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Crystal structure of the LG1-3 region of the laminin alpha2 chain.
19553699
2009
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Compositional and structural requirements for laminin and basement membranes during mouse embryo implantation and gastrulation.
15102706
2004
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Restricted distribution of laminin alpha1 chain in normal adult mouse tissues.
10607917
1999
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
The laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoform.
9151674
1997
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Human laminin A chain (LAMA) gene: chromosomal mapping to locus 18p11.3.
2591971
1989
×
Entrez Id:
284217
Gene Symbol:
LAMA1
LAMA1
0.100
CausalMutation
phenotype
CLINVAR
Shapes, domain organizations and flexibility of laminin and fibronectin, two multifunctional proteins of the extracellular matrix.
6795355
1981