Data on the effect of hypomyelinating leukodystrophy 6 (HLD6)-associated mutations on the TUBB4A properties

Hypomyelinating leukodystrophy (HLD) is genetic demyelinating or dysmyelinating disease and is associated with at least 13 responsible genes. The mutations seem likely cause the functional deficiency of their gene products. HLD4- and HLD5-associated HSPD1 and FAM126A mutations affect biochemical pro...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Yuki Miyamoto, Tomohiro Torii, Kazuko Kawahara, Nanami Hasegawa, Akito Tanoue, Yoichi Seki, Takako Morimoto, Megumi Funakoshi-Tago, Hiroomi Tamura, Keiichi Homma, Masahiro Yamamoto, Junji Yamauchi
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2017-04-01
Sarja:Data in Brief
Aiheet:
HLD6
TUBB4A
Tubulin
Disease-associated mutation
Biochemical property
Linkit:http://www.sciencedirect.com/science/article/pii/S2352340917300434
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