De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
about
Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis.The role of de novo mutations in the development of amyotrophic lateral sclerosis.The Role of Peripheral Myelin Protein 2 in Remyelination.Recent advances in the genetic neuropathies.Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2.A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A family.Screening for SH3TC2, PMP2, and BSCL2 Variants in a Cohort of Chinese Patients with Charcot-Marie-Tooth.Structure and dynamics of a human myelin protein P2 portal region mutant indicate opening of the β barrel in fatty acid binding proteins.
P2860
Q30848999-FB2BAE5A-A83E-4082-9FAA-F7B2DFBC4980Q38676238-4947A24F-AEC5-4F65-BBBB-A0E5B24E45E0Q38817738-32143F44-4EF9-452F-B7A8-3A6BEF81E36FQ38943757-416ADE2F-9E57-4B7C-A42D-8458C6E0CF5FQ41140458-C0BE8D15-C220-4E1E-8772-B9DA4E59AD66Q47564471-63CF7338-274B-448D-8CB5-4A6263674638Q49523386-2FFC276C-EF0C-4E31-8C31-5BEBFF0D53C4Q55424502-A1E12992-8334-4BB1-8112-1E578B71EA50
P2860
De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
@en
type
label
De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
@en
prefLabel
De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
@en
P2093
P2860
P356
P1433
P1476
De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
@en
P2093
Albena Jordanova
Alleene V Strickland
Andreas R Janecke
Els De Vriendt
Feifei Tao
Julia V Wanschitz
Livija Medne
Michael A Gonzalez
Paulius Palaima
Sabrina W Yum
P2860
P304
P356
10.1093/BRAIN/AWW055
P407
P577
2016-03-23T00:00:00Z