WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population.

Autor: Grejtakova, D.¹ daniela.grejtakova@gmail.com, Gabrikova-Dojcakova, D.¹, Boronova, I.¹, Kyjovska, L.², Hubcejova, J.¹, Fecenkova, M.¹, Zigova, M.¹, Priganc, M.¹, Bernasovska, J.¹

Publikováno v: Journal of Genetics. Dec2018, Vol. 97 Issue 5, p1169-1177. 9p.

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

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

Publikováno v: 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 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1ebcd1e25bae4b042acfbc00dd2f6220
https://research.vumc.nl/en/publications/287eb9c5-23d2-4f44-84ef-d0cc93c09501

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