Your browser doesn't support javascript.
loading
Myotonic dystrophy type 1 cosegregating with autosomal dominant polycystic kidney disease type 2.
Nicoletti, Tommaso; Chiurazzi, Pietro; Castori, Marco; Perna, Alessia; Silvestri, Gabriella.
Affiliation
  • Nicoletti T; Dipartimento di Neuroscienze, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Chiurazzi P; UOC Neurologia, Fondazione Policlinico Universitario "A. Gemelli" IRCSS, 00168, Roma, Italy.
  • Castori M; Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Perna A; UOC Genetica Medica, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.
  • Silvestri G; Divisione di Genetica Medica, Fondazione IRCCS-Casa Sollievo della Sofferenza, San Giovanni Rotondo, FG, Italy.
Neurol Sci ; 41(12): 3761-3763, 2020 12.
Article in En | MEDLINE | ID: mdl-32588366
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycystic Kidney, Autosomal Dominant / Myotonic Dystrophy Limits: Humans Language: En Journal: Neurol Sci Journal subject: NEUROLOGIA Year: 2020 Document type: Article Affiliation country: Italy Country of publication: Italy
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polycystic Kidney, Autosomal Dominant / Myotonic Dystrophy Limits: Humans Language: En Journal: Neurol Sci Journal subject: NEUROLOGIA Year: 2020 Document type: Article Affiliation country: Italy Country of publication: Italy