Splicing defects in ABCD1 gene leading to both exon skipping and partial intron retention in X-linked adrenoleukodystrophy Tunisian patient.
about
Splicing defects in ABCD1 gene leading to both exon skipping and partial intron retention in X-linked adrenoleukodystrophy Tunisian patient.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Splicing defects in ABCD1 gene ...... ukodystrophy Tunisian patient.
@en
Splicing defects in ABCD1 gene ...... ukodystrophy Tunisian patient.
@nl
type
label
Splicing defects in ABCD1 gene ...... ukodystrophy Tunisian patient.
@en
Splicing defects in ABCD1 gene ...... ukodystrophy Tunisian patient.
@nl
prefLabel
Splicing defects in ABCD1 gene ...... ukodystrophy Tunisian patient.
@en
Splicing defects in ABCD1 gene ...... ukodystrophy Tunisian patient.
@nl
P2093
P1476
Splicing defects in ABCD1 gene ...... eukodystrophy Tunisian patient
@en
P2093
Amel Ben Chehida
Fakhri Kallabi
Ghada Ben Salah
Hadhami Ben Turkia
Ikhlass Hadj Salem
Leila Keskes
Neji Tebib
P356
10.1016/J.NEURES.2015.03.005
P577
2015-03-31T00:00:00Z