t/laminin

Laminin

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[Congenital muscular dystrophy phenotypes].
Laminin
Polymerizing laminins: Assembly, functions and disorders.
Laminin
Turtle IgD2 preserves an ancestral IgXA-derived XA3–XA4 module in a duplicated and locally remodeled IgD2–IgY constant-region array
Laminin
LAMB2 p.E991K Mutation-Mediated Atherosclerosis in Rabbit.
Laminin
Matrix remodeling plays an etiological role in driving laminin-α2 deficient pathology
Laminin
Hereditary spastic paraplegia in three siblings with distinct genetic mutations.
Laminin
Expanding the phenotypic spectrum of LAMA2-related disorders: Axonal neuropathy in the absence of muscular dystrophy.
Laminin
A Three-Dimensional Biomimetic <em>In Vitro</em> Model to Simulate Schwann Cell-Mediated Peripheral Nerve Repair
Laminin
Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron disease.
Laminin
Expanding the genetic spectrum of neurogenetic disorders in moroccan families by exome sequencing: identification of candidate variants in RYR3, POLR3A, and LAMA2.
Laminin

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