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

Authors :: Hamilton, E. M.
Bertini, E.
Kalaydjieva, L.
Morar, B.
Dojcakova, D.
Diodato, D.
Wolf, N.
Waisfisz, Q.
Abbink, E.
van der Knaap, M. S.
Neurology
Psychiatry
APH - Mental Health
Human genetics
CCA - Cancer biology and immunology
CCA - Cancer Treatment and quality of life
Amsterdam Neuroscience - Cellular & Molecular Mechanisms
Pediatric surgery
Amsterdam Reproduction & Development (AR&D)
Source :: European Journal of Neurology, 25, 31-32. Wiley-Blackwell, Hamilton, E M, Bertini, E, Kalaydjieva, L, Morar, B, Dojcakova, D, Diodato, D, Wolf, N, Waisfisz, Q, Abbink, E & van der Knaap, M S 2018, ' UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC) ', European Journal of Neurology, vol. 25, pp. 31-32 .
Publication Year :: 2018

Language :: English
ISSN :: 13515101
Database :: OpenAIRE
Journal :: European Journal of Neurology, 25, 31-32. Wiley-Blackwell, Hamilton, E M, Bertini, E, Kalaydjieva, L, Morar, B, Dojcakova, D, Diodato, D, Wolf, N, Waisfisz, Q, Abbink, E & van der Knaap, M S 2018, ' UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC) ', European Journal of Neurology, vol. 25, pp. 31-32 .
Accession number :: edsair.dedup.wf.001..1ebcd1e25bae4b042acfbc00dd2f6220

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