A response to Dr. Alzahrani's letter to the editor regarding the mechanism underlying fibrochondrogenesis

被引：1

作者：

Akawi, Nadia A. ^{[1
]}

Ali, Bassam R. ^{[1
]}

Al-Gazali, Lihadh ^{[2
]}

机构：

[1] United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Pathol, Al Ain, U Arab Emirates

[2] United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Paediat, Al Ain, U Arab Emirates

来源：

GENE | 2013年 / 528卷 / 02期

关键词：

COL11A1;

D O I：

10.1016/j.gene.2013.07.038

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：367 / 368

页数：2

共 3 条

[1] Clinical and molecular analysis of UAE fibrochondrogenesis patients expands the phenotype and reveals two COL11A1 homozygous null mutations [J].

Akawi, N. A. ;

Al-Gazali, L. ;

Ali, B. R. .

CLINICAL GENETICS, 2012, 82 (02) :147-156

[2] Molecular pathogenesis of fibrochondrogenesis: Is it really simple COL11A1 deficiency? [J].

Alzahrani, Fatema ;

Alshammari, Muneera J. ;

Alkuraya, Fowzan S. .

GENE, 2012, 511 (02) :480-481

[3] A FIBRILLAR COLLAGEN GENE, COL11A1, IS ESSENTIAL FOR SKELETAL MORPHOGENESIS [J].

LI, Y ;

LACERDA, DA ;

WARMAN, ML ;

BEIER, DR ;

YOSHIOKA, H ;

NINOMIYA, Y ;

OXFORD, JT ;

MORRIS, NP ;

ANDRIKOPOULOS, K ;

RAMIREZ, F ;

WARDELL, BB ;

LIFFERTH, GD ;

TEUSCHER, C ;

WOODWARD, SR ;

TAYLOR, BA ;

SEEGMILLER, RE ;

OLSEN, BR .

CELL, 1995, 80 (03) :423-430

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