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588P Phenotype variability and natural history of X-linked myopathy with excessive autophagy running head: natural history of XMEA.

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Title: 588P Phenotype variability and natural history of X-linked myopathy with excessive autophagy running head: natural history of XMEA.
Authors: Fernández-Eulate, G.1 (AUTHOR), Alfieri, G.2 (AUTHOR), Spinazzi, M.3 (AUTHOR), Ackermann-Bonan, I.4 (AUTHOR), Duval, F.5 (AUTHOR), Solé, G.5 (AUTHOR), Caillon, F.6 (AUTHOR), Mercier, S.7 (AUTHOR), Pereon, Y.8 (AUTHOR), Magot, A.8 (AUTHOR), Pegat, A.9 (AUTHOR), Salort-Campana, E.10 (AUTHOR), Gorokhova, S.11 (AUTHOR), Krahn, M.11 (AUTHOR), Biancalana, V.12 (AUTHOR), Evangelista, T.1 (AUTHOR), Behin, A.1 (AUTHOR), Metay, C.13 (AUTHOR), Stojkovic, T.1 (AUTHOR)
Source: Neuromuscular Disorders. 2024 Supplement 1, Vol. 43, pN.PAG-N.PAG. 1p.
Database: Academic Search Ultimate
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  Availability: 0
Header DbId: asn
DbLabel: Academic Search Ultimate
An: 180115120
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: 588P Phenotype variability and natural history of X-linked myopathy with excessive autophagy running head: natural history of XMEA.
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  Data: <searchLink fieldCode="JN" term="%22Neuromuscular+Disorders%22">Neuromuscular Disorders</searchLink>. 2024 Supplement 1, Vol. 43, pN.PAG-N.PAG. 1p.
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              Text: 2024 Supplement 1
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