Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease-Reference-Cited by-同舟云学术

Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease

Published:1996-11 Issue:3 Volume:14 Page:345-347
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Salomon Rémi,Attié Tania,Pelet Anna,Bidaud Christelle,Eng Charis,Amiel Jeanne,Sarnacki Sabine,Goulet Olivier,Ricour Claude,Nihoul-Fékété Claire,Munnich Arnold,Lyonnet Stanislas

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1196-345.pdf

Reference30 articles.

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2. Bolande, R. The neurocristopathies ; A unifyng concept of disease arising in neural crest maldevelopment. Hum. Path. 5, 409–429 (1973).

3. Badner, J. & Chakravarty, A., Syndrome and Hirschsprung Disease : Evidence for pleiotropic effects of a single dominant gene. Am. J. Med. Genet. 35, 100–104 (1990).

4. Passarge, E. The genetics of Hirschsprung disease. N. Engl. J. Med. 276, 138–143 (1987).

5. Angrist, M. et al. A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10. Nature Genet. 4, 351–356 (1993).

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