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2000 | 2 |
2001 | 1 |
2024 | 0 |
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PMP22 related congenital hypomyelination neuropathy.
J Neurol Neurosurg Psychiatry. 2001 Jan;70(1):123-6. doi: 10.1136/jnnp.70.1.123.
J Neurol Neurosurg Psychiatry. 2001.
PMID: 11118262
Free PMC article.
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero.
Fabrizi GM, Taioli F, Cavallaro T, Rigatelli F, Simonati A, Mariani G, Perrone P, Rizzuto N.
Fabrizi GM, et al. Among authors: rigatelli f.
Acta Neuropathol. 2000 Sep;100(3):299-304. doi: 10.1007/s004019900175.
Acta Neuropathol. 2000.
PMID: 10965800
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Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of italian families with Marfan syndrome.
Mottes M, Mirandola S, Rigatelli F, Zolezzi F, Lisi V, Gordon D, Pignatti PF.
Mottes M, et al. Among authors: rigatelli f.
Hum Hered. 2000 May-Jun;50(3):175-9. doi: 10.1159/000022910.
Hum Hered. 2000.
PMID: 10686496
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