Literature DB >> 26819212

Erratum to: Non-Ceruloplasmin Copper Distincts Subtypes in Alzheimer's Disease: a Genetic Study of ATP7B Frequency.

Rosanna Squitti1,2, Mariacarla Ventriglia3, Massimo Gennarelli4,5, Nicola A Colabufo6, Imane Ghafir El Idrissi7, Serena Bucossi8, Stefania Mariani3, Mauro Rongioletti9, Orazio Zanetti10, Chiara Congiu10, Paolo M Rossini11, Cristian Bonvicini4.   

Abstract

Entities:  

Year:  2017        PMID： 26819212     DOI： 10.1007/s12035-016-9734-4

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN： 0893-7648            Impact factor:   5.590


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  1 in total

1.  A case of a mild Wolfram Syndrome with concomitant ATP7B mutation.

Authors:  R Squitti; G Cerchiaro; I Giovannoni; P Francalanci; M Siotto; P Maffei; C Ricordi; M C Rongioletti
Journal:  CellR4 Repair Replace Regen Reprogram       Date:  2019-08-28
  1 in total

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