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...

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Bibliografiska uppgifter
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: Elsevier 2017-04-01
Serie:Data in Brief
Ämnen:
HLD6
TUBB4A
Tubulin
Disease-associated mutation
Biochemical property
Länkar:http://www.sciencedirect.com/science/article/pii/S2352340917300434
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