UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC)

E. M. Hamilton; E. Bertini; L. Kalaydjieva; B. Morar; D. Dojcakova; D. Diodato; N. Wolf; Q. Waisfisz; E. Abbink; M. S. van der Knaap

UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC)

E. M. Hamilton, E. Bertini, L. Kalaydjieva, B. Morar, D. Dojcakova, D. Diodato, N. Wolf, Q. Waisfisz, E. Abbink, M. S. van der Knaap

Research output: Contribution to journal › Meeting Abstract › Academic

Original language	English
Pages (from-to)	31-32
Journal	European journal of neurology
Volume	25
Publication status	Published - Jun 2018

Cite this

@article{592c1d4a7c6c48bb8137be4ea2bea27c,

title = "UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC)",

author = "Hamilton, {E. M.} and E. Bertini and L. Kalaydjieva and B. Morar and D. Dojcakova and D. Diodato and N. Wolf and Q. Waisfisz and E. Abbink and {van der Knaap}, {M. S.}",

year = "2018",

month = jun,

language = "English",

volume = "25",

pages = "31--32",

journal = "European journal of neurology",

issn = "1351-5101",

publisher = "Wiley-Blackwell",

}

TY - JOUR

T1 - UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC)

AU - Hamilton, E. M.

AU - Bertini, E.

AU - Kalaydjieva, L.

AU - Morar, B.

AU - Dojcakova, D.

AU - Diodato, D.

AU - Wolf, N.

AU - Waisfisz, Q.

AU - Abbink, E.

AU - van der Knaap, M. S.

PY - 2018/6

Y1 - 2018/6

M3 - Meeting Abstract

SN - 1351-5101

VL - 25

SP - 31

EP - 32

JO - European journal of neurology

JF - European journal of neurology

ER -