A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia

[1]  T. Pemberton,et al.  A novel Gln358Glu mutation in ectodysplasin A associated with X‐linked dominant incisor hypodontia , 2007, American journal of medical genetics. Part A.

[2]  Lin He,et al.  A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia , 2006, Journal of Human Genetics.

[3]  P. Jagodziński,et al.  Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis , 2006, Journal of Human Genetics.

[4]  Torsten Schwede,et al.  BIOINFORMATICS Bioinformatics Advance Access published November 12, 2005 The SWISS-MODEL Workspace: A web-based environment for protein structure homology modelling , 2022 .

[5]  Minhong Yan,et al.  The crystal structures of EDA-A1 and EDA-A2: splice variants with distinct receptor specificity. , 2003, Structure.

[6]  E. Chautard-Freire-Maia,et al.  X‐linked hypohidrotic ectodermal dysplasia mutations in Brazilian families , 2003, American journal of medical genetics. Part A.

[7]  G. Gamba,et al.  [Initial sequence and analysis of the human genome]. , 2001, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.

[8]  J. Tschopp,et al.  Mutations Leading to X-linked Hypohidrotic Ectodermal Dysplasia Affect Three Major Functional Domains in the Tumor Necrosis Factor Family Member Ectodysplasin-A* , 2001, The Journal of Biological Chemistry.

[9]  J. V. Moran,et al.  Initial sequencing and analysis of the human genome. , 2001, Nature.

[10]  H. Vastardis.  The genetics of human tooth agenesis: new discoveries for understanding dental anomalies. , 2000, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.

[11]  J C Murray,et al.  Pediatrics and , 1998 .

[12]  J. Seidman,et al.  A human MSX1 homeodomain missense mutation causes selective tooth agenesis , 1996, Nature Genetics.

[13]  A A Schäffer,et al.  Faster sequential genetic linkage computations. , 1993, American journal of human genetics.

[14]  P. Patel,et al.  Mutation of PAX9 is associated with oligodontia , 2000, Nature Genetics.

[15]  A. Symons,et al.  Anomalies associated with hypodontia of the permanent lateral incisor and second premolar. , 1993, The Journal of clinical pediatric dentistry.

[16]  C. Choi.  The Crystal Structures , 1977 .

[17]  H. Lipson.  Crystal Structures , 1949, Nature.