Tendon Is Covered by a Basement Membrane Epithelium That Is Required for Cell Retention and the Prevention of Adhesion Formation.

Intracerebral hemorrhage in a young man.

Acute urinary retention due to a novel collagen COL4A! mutation.

COL4A1 Mutation in Preterm Intraventricular Hemorrhage.

Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume.

COL4A1 Mutation in Two Preterm Siblings with Antenatal Onset of Parenchymal Hemorrhage.

Abnormal Expression of Collagen IV in Lens Activates Unfolded Protein Response Resulting in Cataract.

Intracerebral Hemorrhage and COL4A1 Mutations, from Preterm Infants to Adult Patients.

Clinical and brain MRI follow-up study of a family with COL4A1 mutation.

COL4A1 Mutation in Axenfeld–Rieger Anomaly with Leukoencephalopathy and Stroke.

COL4A1 Mutation in a Patient With Sporadic, Recurrent Intracerebral Hemorrhage.

Col4a1 mutation causes endoplasmic reticulum stress and genetically modifiable ocular dysgenesis.

Type IV Procollagen Missense Mutations Associated With Defects of the Eye, Vascular Stability, the Brain, Kidney Function and Embryonic or Postnatal Viability in the Mouse, Mus musculus: An Extension of the Col4a1 Allelic Series and the Identification of the First Two Col4a2 Mutant Alleles.

Role of COL4A1 in Small-Vessel Disease and Hemorrhagic Stroke

Role of COL4A1 in Small-Vessel Disease and Hemorrhagic Stroke

Neonatal Porencephaly and Adult Stroke Related to Mutations in Collagen IV A1

Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly

Mutations in Col4a1 Cause Perinatal Cerebral Hemorrhage and Porencephaly

Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly.

Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly.