| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Hereditary Neuropathy v2.47 | LAMA2 | Zornitza Stark Marked gene: LAMA2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy v2.47 | LAMA2 | Zornitza Stark Gene: lama2 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy v2.47 | LAMA2 | Zornitza Stark Classified gene: LAMA2 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy v2.47 | LAMA2 | Zornitza Stark Gene: lama2 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy v2.46 | LAMA2 |
Zornitza Stark gene: LAMA2 was added gene: LAMA2 was added to Hereditary Neuropathy. Sources: Literature Mode of inheritance for gene: LAMA2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: LAMA2 were set to 41765988; 37206914; 35868801 Phenotypes for gene: LAMA2 were set to LAMA2-related muscular dystrophy MONDO:0100228 Review for gene: LAMA2 was set to GREEN Added comment: Classically a muscular dystrophy, however PMID 37206914 reports 19 individuals from 17 families with autosomal recessive limb‑girdle muscular dystrophy (LGMD R23) in which 46.7 % have motor neuropathy; and additional reports identified. Sources: Literature |
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