Literature DB >> 9359036

Mutations in Hirschsprung disease: when does a mutation contribute to the phenotype.

R M Hofstra1, J Osinga, C H Buys.   

Abstract

Hirschsprung disease is a congenital disorder clinically characterized by the absence of colonic ganglia and genetically by extensive heterogeneity. Genes involved include RET, GDNF, EDNRB and EDN3. Mutations of these genes may give dominant, recessive, or polygenic patterns of inheritance. In particular in the case of missense mutations, it is therefore far from easy to assess whether a given mutation will contribute to the phenotype. We discuss criteria for such an assessment and pay special attention to functional assays. The interpretation of mutations as contributing to a disease phenotype or as merely representing a rare polymorphism has direct clinical consequences. Hirschsprung disease with major and modifying sequence variants in a variety of genes might well serve as a model for the many complex disorders for which the search for genes involved has only just been initiated.

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Year:  1997        PMID: 9359036

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  17 in total

1.  A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.

Authors:  S Bolk; A Pelet; R M Hofstra; M Angrist; R Salomon; D Croaker; C H Buys; S Lyonnet; A Chakravarti
Journal:  Proc Natl Acad Sci U S A       Date:  2000-01-04       Impact factor: 11.205

Review 2.  Developmental disorders of the enteric nervous system.

Authors:  R P Kapur
Journal:  Gut       Date:  2000-12       Impact factor: 23.059

3.  Association study of PHOX2B as a candidate gene for Hirschsprung's disease.

Authors:  M Garcia-Barceló; M H Sham; V C H Lui; B L S Chen; J Ott; P K H Tam
Journal:  Gut       Date:  2003-04       Impact factor: 23.059

Review 4.  Genetic interactions and modifier genes in Hirschsprung's disease.

Authors:  Adam S Wallace; Richard B Anderson
Journal:  World J Gastroenterol       Date:  2011-12-07       Impact factor: 5.742

5.  1998 ASHG presidential address. Making genomic medicine a reality.

Authors:  A L Beaudet
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025

6.  Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease.

Authors:  B Herbarth; V Pingault; N Bondurand; K Kuhlbrodt; I Hermans-Borgmeyer; A Puliti; N Lemort; M Goossens; M Wegner
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-28       Impact factor: 11.205

7.  Novel mutations at RET ligand genes preventing receptor activation are associated to Hirschsprung's disease.

Authors:  Macarena Ruiz-Ferrer; Ana Torroglosa; Berta Luzón-Toro; Raquel M Fernández; Guillermo Antiñolo; Lois M Mulligan; Salud Borrego
Journal:  J Mol Med (Berl)       Date:  2011-01-05       Impact factor: 4.599

8.  The sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosis.

Authors:  B Mograbi; R Bocciardi; I Bourget; T Juhel; D Farahi-Far; G Romeo; I Ceccherini; B Rossi
Journal:  Mol Cell Biol       Date:  2001-10       Impact factor: 4.272

9.  Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant.

Authors:  Maran J W Berends; Ying Wu; Rolf H Sijmons; Rob G J Mensink; Tineke van der Sluis; Jannet M Hordijk-Hos; Elisabeth G E de Vries; Harry Hollema; Arend Karrenbeld; Charles H C M Buys; Ate G J van der Zee; Robert M W Hofstra; Jan H Kleibeuker
Journal:  Am J Hum Genet       Date:  2002-01       Impact factor: 11.025

10.  In vivo imaging of enteric neurogenesis in the deep tissue of mouse small intestine.

Authors:  Kei Goto; Go Kato; Isao Kawahara; Yi Luo; Koji Obata; Hiromi Misawa; Tatsuya Ishikawa; Hiroki Kuniyasu; Junich Nabekura; Miyako Takaki
Journal:  PLoS One       Date:  2013-01-31       Impact factor: 3.240

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