muscle
|
• mice exhibit a phenotype similar to other mice homozygous for other mutant alleles of Lama2
|
|
• mice exhibit a phenotype similar to other mice homozygous for other mutant alleles of Lama2
|
behavior/neurological
|
• mice exhibit a phenotype similar to other mice homozygous for other mutant alleles of Lama2
|
skeleton
|
• mice exhibit a phenotype similar to other mice homozygous for other mutant alleles of Lama2
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
| congenital merosin-deficient muscular dystrophy 1A | DOID:0110636 |
OMIM:607855 |
J:56803 | |


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