Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutation
about
A structural variant in the 5'-flanking region of the TWIST2 gene affects melanocyte development in belted cattleRecurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say SyndromesFocal facial dermal dysplasia type 4: identification of novel CYP26C1 mutations in unrelated patients.
P2860
Setleis syndrome: clinical, molecular and structural studies of the first TWIST2 missense mutation
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Setleis syndrome: clinical, mo ...... first TWIST2 missense mutation
@ast
Setleis syndrome: clinical, mo ...... first TWIST2 missense mutation
@en
type
label
Setleis syndrome: clinical, mo ...... first TWIST2 missense mutation
@ast
Setleis syndrome: clinical, mo ...... first TWIST2 missense mutation
@en
prefLabel
Setleis syndrome: clinical, mo ...... first TWIST2 missense mutation
@ast
Setleis syndrome: clinical, mo ...... first TWIST2 missense mutation
@en
P2093
P2860
P356
P1433
P1476
Setleis syndrome: clinical, mo ...... first TWIST2 missense mutation
@en
P2093
Aneel K Aggarwal
Beom Hee Lee
Carmen L Cadilla
Hilal Ozgur
Irina Nazarenko
Mehmet Bekerecioglu
R Ozgur Rosti
Robert J Desnick
Sacide Pehlivan
Z Oya Uyguner
P2860
P304
P356
10.1111/CGE.12539
P577
2014-11-19T00:00:00Z