A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk.

A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk.

Item
http://www.wikidata.org/entity/Q48070924
Form and function: the laminin family of heterotrimersThe laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoformPrimary structure, developmental expression, and immunolocalization of the murine laminin alpha4 chainMolecular pathology of the cutaneous basement membrane zone.Paraneoplastic cicatricial pemphigoid.Laminins: structure and genetic regulation.The genetics of human skin disease.Roles for laminin in embryogenesis: exencephaly, syndactyly, and placentopathy in mice lacking the laminin alpha5 chainDetection of novel LAMC2 mutations in Herlitz junctional epidermolysis BullosaMolecular genetics of ameloblast cell lineage.Laminin: loss-of-function studies.Kidney development and perspectives for organ engineering.The Role of Integrin α6 (CD49f) in Stem Cells: More than a Conserved Biomarker.Lessons from skin blistering: molecular mechanisms and unusual patterns of inheritance?The role of laminins in basement membrane function.Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.
P2860

A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk.

Item
http://www.wikidata.org/entity/Q48070924
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh
1995年學術文章
@zh-hant
name
A homozygous nonsense mutation ...... exclusion in a fetus at risk.
@en
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5
@nl
type
label
A homozygous nonsense mutation ...... exclusion in a fetus at risk.
@en
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5
@nl
prefLabel
A homozygous nonsense mutation ...... exclusion in a fetus at risk.
@en
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5
@nl
P1433
P1476
P2093
P304
P31
P356
P433
P478
P577
P698
P356
P1433
P1476
A homozygous nonsense mutation ...... exclusion in a fetus at risk.
@en
P2093
P304
P31
P356
P433
P478
P577
P698