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ACTN2 mutations cause "Multiple structured Core Disease" (MsCD).
Acta Neuropathol. 2019 Mar;137(3):501-519. doi: 10.1007/s00401-019-01963-8. Epub 2019 Jan 30.
Acta Neuropathol. 2019.
PMID: 30701273
Free PMC article.
Homozygous TRPV4 mutation causes congenital distal spinal muscular atrophy and arthrogryposis.
Velilla J, Marchetti MM, Toth-Petroczy A, Grosgogeat C, Bennett AH, Carmichael N, Estrella E, Darras BT, Frank NY, Krier J, Gaudet R, Gupta VA.
Velilla J, et al. Among authors: marchetti mm.
Neurol Genet. 2019 Mar 7;5(2):e312. doi: 10.1212/NXG.0000000000000312. eCollection 2019 Apr.
Neurol Genet. 2019.
PMID: 31041394
Free PMC article.
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