A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency.
about
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh
2017年學術文章
@zh-hant
name
A novel PAX1 null homozygous m ...... ere combined immunodeficiency.
@en
A novel PAX1 null homozygous m ...... ere combined immunodeficiency.
@nl
type
label
A novel PAX1 null homozygous m ...... ere combined immunodeficiency.
@en
A novel PAX1 null homozygous m ...... ere combined immunodeficiency.
@nl
prefLabel
A novel PAX1 null homozygous m ...... ere combined immunodeficiency.
@en
A novel PAX1 null homozygous m ...... ere combined immunodeficiency.
@nl
P2093
P2860
P356
P1433
P1476
A novel PAX1 null homozygous m ...... ere combined immunodeficiency.
@en
P2093
A Barilaro
A L Putignano
B Porfirio
G L Capone
I Paganini
P2860
P304
P356
10.1111/CGE.13085
P50
P577
2017-06-28T00:00:00Z