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Phenotypic manifestations of the OCTN2 V295X mutation: Sudden infant death and carnitine-responsive cardiomyopathy in Roma families

✍ Scribed by Melegh, Béla ;Bene, Judit ;Mogyorósy, Gábor ;Havasi, Viktória ;Komlósi, Katalin ;Pajor, László ;Oláh, Éva ;Kispál, Gyula ;Sumegi, Balázs ;Méhes, Károly


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
346 KB
Volume
131A
Category
Article
ISSN
0148-7299

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