Phenotypic heterogeneity of movement disorders due to intracranial calcifications with or without SLC20A2 mutations

Carecchio; M (Carecchio; M. ) Varrasi; C (Varrasi; C. ) Barzaghi; C (Barzaghi; C. ) Magistrelli; L (Magistrelli; L. ) Comi; Cristoforo COMI; C. ) Garavaglia; B (Garavaglia; B. ) Cantello; Roberto CANTELLO

Phenotypic heterogeneity of movement disorders due to intracranial calcifications with or without SLC20A2 mutations

Carecchio
, M (Carecchio
, M. ) Varrasi
, C (Varrasi
, C. ) Barzaghi
, C (Barzaghi
, C. ) Magistrelli
, L (Magistrelli
, L. ) Comi
, Cristoforo COMI
, C. ) Garavaglia
, B (Garavaglia
, B. ) Cantello
, Roberto CANTELLO

Department of Translational Medicine

Research output: Contribution to journal › Article › peer-review

Original language	Italian
Journal	Movement Disorders
Publication status	Published - 1 Jan 2014

Cite this

@article{b8c1b8fd71bc46348a6c70f87177f4da,

title = "Phenotypic heterogeneity of movement disorders due to intracranial calcifications with or without SLC20A2 mutations",

author = "Carecchio and M (Carecchio and Varrasi, \{M. )\} and C (Varrasi and Barzaghi, \{C. )\} and C (Barzaghi and Magistrelli, \{C. )\} and L (Magistrelli and Comi, \{L. )\} and Cristoforo COMI and Garavaglia, \{C. )\} and B (Garavaglia and Cantello, \{B. )\} and Roberto CANTELLO",

year = "2014",

month = jan,

day = "1",

language = "Italian",

journal = "Movement Disorders",

issn = "1531-8257",

publisher = "John Wiley \& Sons Inc.",

}

TY - JOUR

T1 - Phenotypic heterogeneity of movement disorders due to intracranial calcifications with or without SLC20A2 mutations

AU - Carecchio, null

AU - (Carecchio, M

AU - Varrasi, M. )

AU - (Varrasi, C

AU - Barzaghi, C. )

AU - (Barzaghi, C

AU - Magistrelli, C. )

AU - (Magistrelli, L

AU - Comi, L. )

AU - COMI, Cristoforo

AU - Garavaglia, C. )

AU - (Garavaglia, B

AU - Cantello, B. )

AU - CANTELLO, Roberto

PY - 2014/1/1

Y1 - 2014/1/1

UR - https://iris.uniupo.it/handle/11579/103698

M3 - Articolo in rivista

SN - 1531-8257

JO - Movement Disorders

JF - Movement Disorders

ER -

Phenotypic heterogeneity of movement disorders due to intracranial calcifications with or without SLC20A2 mutations

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Cite this