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LAMA2
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Body Atlas
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Heart atrium
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Omental adipose tissue
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Hind limb skeletal muscle expression from laminin alpha 2 chain deficient mice
Laminin-deficient muscular dystrophy, dy/dy diaphragm
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Most Relevant Literature
Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosi…
Peripheral nerve injury in LAMA2-related congenital muscular dystrophy patients].
Merosin-deficient congenital muscular dystrophy: A novel homozygous mutation in the laminin-2 gene.
LAMA2-related congenital muscular dystrophy complicated by West syndrome.
Atypical phenotype in two patients with LAMA2 mutations.
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Retrospective Natural History Study of Infants and Toddlers With LAMA2-CMD
The Natural History of Patients With Mutations in SEPN1 (SELENON) or LAMA2
LAMA2-related Muscular Dystrophy Brain Study
A Study to Test Lung Stretch Therapy (Hyperinsufflation) in Children With Collagen VI Muscular Dystr…
Congenital Muscle Disease Study of Patient and Family Reported Medical Information
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