Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB

Michael J. Keogh; Angela Pyle; Daniyal Daud; Helen Griffin; Konstantinos Douroudis; Gail Eglon; James Miller; Rita Horvath; Patrick F. Chinnery

doi:10.1212/WNL.0000000000001517

Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB

Michael J. Keogh, Angela Pyle, Daniyal Daud, Helen Griffin, Konstantinos Douroudis, Gail Eglon, James Miller, Rita Horvath, Patrick F. Chinnery^*

^*Corresponding author for this work

Research output: Contribution to journal › Comment/debate

19 Citations (Scopus)

Original language	English
Pages (from-to)	1818-1820
Number of pages	3
Journal	Neurology
Volume	84
Issue number	17
DOIs	https://doi.org/10.1212/WNL.0000000000001517
Publication status	Published - 28 Apr 2015
Externally published	Yes

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title = "Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB",

author = "Keogh, \{Michael J.\} and Angela Pyle and Daniyal Daud and Helen Griffin and Konstantinos Douroudis and Gail Eglon and James Miller and Rita Horvath and Chinnery, \{Patrick F.\}",

year = "2015",

month = apr,

day = "28",

doi = "10.1212/WNL.0000000000001517",

language = "English",

volume = "84",

pages = "1818--1820",

journal = "Neurology",

issn = "0028-3878",

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}

TY - JOUR

T1 - Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB

AU - Keogh, Michael J.

AU - Pyle, Angela

AU - Daud, Daniyal

AU - Griffin, Helen

AU - Douroudis, Konstantinos

AU - Eglon, Gail

AU - Miller, James

AU - Horvath, Rita

AU - Chinnery, Patrick F.

PY - 2015/4/28

Y1 - 2015/4/28

UR - https://www.scopus.com/pages/publications/84929119597

U2 - 10.1212/WNL.0000000000001517

DO - 10.1212/WNL.0000000000001517

M3 - Comment/debate

C2 - 25832657

AN - SCOPUS:84929119597

SN - 0028-3878

VL - 84

SP - 1818

EP - 1820

JO - Neurology

JF - Neurology

IS - 17

ER -

Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB

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