Human Genome Epidemiology Literature Finder
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Query Trace: Atrophy and UFM1[original query] |
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UFM1 founder mutation in the Roma population causes recessive variant of H-ABC. Neurology 2017 Sep . Hamilton Eline M C, Bertini Enrico, Kalaydjieva Luba, Morar Bharti, Doj?áková Dana, Liu Judy, Vanderver Adeline, Curiel Julian, Persoon Claudia M, Diodato Daria, Pinelli Lorenzo, van der Meij Nathalie L, Plecko Barbara, Blaser Susan, Wolf Nicole I, Waisfisz Quinten, Abbink Truus E M, van der Knaap Marjo S, |
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- Page last updated:Apr 22, 2024
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