Hypotonic male infant and MCT8 deficiency - a diagnosis to think about.
about
BDE-99 impairs differentiation of human and mouse NPCs into the oligodendroglial lineage by species-specific modes of actionEndocrine disorders and the neurologic manifestations.Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies.The Value of Comprehensive Thyroid Function Testing and Family History for Early Diagnosis of MCT8 Deficiency.
P2860
Hypotonic male infant and MCT8 deficiency - a diagnosis to think about.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh-hant
name
Hypotonic male infant and MCT8 deficiency - a diagnosis to think about.
@en
Hypotonic male infant and MCT8 deficiency - a diagnosis to think about.
@nl
type
label
Hypotonic male infant and MCT8 deficiency - a diagnosis to think about.
@en
Hypotonic male infant and MCT8 deficiency - a diagnosis to think about.
@nl
prefLabel
Hypotonic male infant and MCT8 deficiency - a diagnosis to think about.
@en
Hypotonic male infant and MCT8 deficiency - a diagnosis to think about.
@nl
P2093
P2860
P356
P1433
P1476
Hypotonic male infant and MCT8 deficiency - a diagnosis to think about.
@en
P2093
Andrés Nascimento
Carlos Ortez
Filipa Rodrigues
Jaume Colomer
Joana Grenha
Judith Armstrong
Monica M-Belinchón
P2860
P2888
P356
10.1186/1471-2431-14-252
P577
2014-10-04T00:00:00Z
P5875
P6179
1008265662