Mutations in INPP5K, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment
about
Genetic and Clinical Advances of Congenital Muscular Dystrophy.Hybrid Method Based on Information Gain and Support Vector Machine for Gene Selection in Cancer Classification.The inositol 5-phosphatase INPP5K participates in the fine control of ER organizationCognitive impairment in neuromuscular diseases: A systematic review
P2860
Mutations in INPP5K, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment
description
2017 nî lūn-bûn
@nan
2017 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
name
Mutations in INPP5K, Encoding ...... and Mild Cognitive Impairment
@ast
Mutations in INPP5K, Encoding ...... and Mild Cognitive Impairment
@en
type
label
Mutations in INPP5K, Encoding ...... and Mild Cognitive Impairment
@ast
Mutations in INPP5K, Encoding ...... and Mild Cognitive Impairment
@en
prefLabel
Mutations in INPP5K, Encoding ...... and Mild Cognitive Impairment
@ast
Mutations in INPP5K, Encoding ...... and Mild Cognitive Impairment
@en
P2093
P2860
P50
P1476
Mutations in INPP5K, Encoding ...... and Mild Cognitive Impairment
@en
P2093
Andreas Roos
Benedikt Schoser
Birgit Ertl-Wagner
Caroline Sewry
Carsten G Bönnemann
Chiara Marini Bettolo
Christian De Goede
Christopher J Munn
Cristiane Araújo Martins Moreno
P2860
P304
P356
10.1016/J.AJHG.2017.01.024
P407
P50
P577
2017-02-08T00:00:00Z