Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1-Reference-Cited by-同舟云学术

Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1

Published:2018-04-30 Issue:8 Volume:26 Page:1132-1142
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Brock Stefanie,Stouffs Katrien,Scalais Emmanuel,D’Hooghe Marc,Keymolen Kathelijn,Guerrini Renzo,Dobyns William B.^ORCID,Di Donato Nataliya^ORCID,Jansen Anna C.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/s41431-018-0146-y.pdf

Reference39 articles.

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3. Rommens JM, Durocher F, McArthur J, et al. Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21. Genomics. 1995;28:530–42.

4. Friedmann M, Holth LT, Zoghbi HY, Reeves R. Organization, inducible-expression and chromosome localization of the human HMG-I(Y) nonhistone protein gene. Nucleic Acids Res. 1993;21:4259–67.

5. Draberova E, Sulimenko V, Vinopal S, et al. Differential expression of human gamma-tubulin isotypes during neuronal development and oxidative stress points to a gamma-tubulin-2 prosurvival function. FASEB J. 2017;31:1828–46.

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