Congenital disorder of glycosylation type Ia in a Malaysian family: clinical outcome and description of a novel PMM2 mutation.
about
Congenital disorder of glycosylation type Ia in a Malaysian family: clinical outcome and description of a novel PMM2 mutation.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Congenital disorder of glycosy ...... tion of a novel PMM2 mutation.
@en
Congenital disorder of glycosy ...... tion of a novel PMM2 mutation.
@nl
type
label
Congenital disorder of glycosy ...... tion of a novel PMM2 mutation.
@en
Congenital disorder of glycosy ...... tion of a novel PMM2 mutation.
@nl
prefLabel
Congenital disorder of glycosy ...... tion of a novel PMM2 mutation.
@en
Congenital disorder of glycosy ...... tion of a novel PMM2 mutation.
@nl
P2093
P2860
P921
P1476
Congenital disorder of glycosy ...... ption of a novel PMM2 mutation
@en
P2093
P2860
P2888
P356
10.1007/S10545-009-1031-1
P478
32 Suppl 1
P577
2009-01-26T00:00:00Z