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Expanding the Molecular Spectrum of HK1-Related Charcot-Marie-Tooth Disease, Type 4G; the First Report in Iran.
Arch Iran Med. 2023 May 1;26(5):279-284. doi: 10.34172/aim.2023.43.
Arch Iran Med. 2023.
PMID: 38301092
Free PMC article.
Bi-allelic loss of function variant in the NRCAM gene is associated with motor-predominant axonal polyneuropathy; the second report.
Elahi Z, Soveyzi M, Nafissi S, Nilipour Y, Goleyjani Moghadam M, Keshavarz E, Kariminejad A, Najmabadi H, Fattahi Z.
Elahi Z, et al. Among authors: goleyjani moghadam m.
Mol Genet Genomic Med. 2023 Apr;11(4):e2131. doi: 10.1002/mgg3.2131. Epub 2023 Jan 6.
Mol Genet Genomic Med. 2023.
PMID: 36606341
Free PMC article.
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