A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome.
about
A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on December 2016
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
A novel intronic splice site t ...... a family with Barth syndrome.
@en
A novel intronic splice site t ...... a family with Barth syndrome.
@nl
type
label
A novel intronic splice site t ...... a family with Barth syndrome.
@en
A novel intronic splice site t ...... a family with Barth syndrome.
@nl
prefLabel
A novel intronic splice site t ...... a family with Barth syndrome.
@en
A novel intronic splice site t ...... a family with Barth syndrome.
@nl
P2093
P2860
P356
P1476
A novel intronic splice site t ...... a family with Barth syndrome.
@en
P2093
A Morkūnienė
E Benušienė
L Ambrozaitytė
M Bakšienė
V Kučinskas
P2860
P304
P356
10.1515/BJMG-2016-0043
P577
2016-12-01T00:00:00Z