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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1965 | 1 |
1966 | 1 |
2017 | 1 |
2024 | 0 |
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HEREDITARY OCCURRENCE OF NEMALINE MYOPATHY.
Arch Neurol. 1965 Aug;13:155-9. doi: 10.1001/archneur.1965.00470020045006.
Arch Neurol. 1965.
PMID: 14315666
No abstract available.
Nemaline myopathy. The origin of nemaline structures.
Gonatas NK, Shy GM, Godfrey EH.
Gonatas NK, et al.
N Engl J Med. 1966 Mar 10;274(10):535-9. doi: 10.1056/NEJM196603102741002.
N Engl J Med. 1966.
PMID: 5908457
No abstract available.
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Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.
Konersman CG, Freyermuth F, Winder TL, Lawlor MW, Lagier-Tourenne C, Patel SB.
Konersman CG, et al.
Mol Genet Genomic Med. 2017 Nov;5(6):678-691. doi: 10.1002/mgg3.325. Epub 2017 Aug 21.
Mol Genet Genomic Med. 2017.
PMID: 29178646
Free PMC article.
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