(Q41012202)

25 September 2017

title

Mutational analysis of the endothelin-B receptor gene in Japanese Hirschsprung's disease (English)

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25 September 2017

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Inoue M

1

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25 September 2017

Hosoda K

2

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25 September 2017

Imura K

3

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25 September 2017

Kamata S

4

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25 September 2017

Fukuzawa M

5

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25 September 2017

Nakao K

6

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25 September 2017

Okada A

7

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25 September 2017

language of work or name

English

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publication date

1 August 1998

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Journal of Pediatric Surgery

25 September 2017

published in

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25 September 2017

volume

33

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25 September 2017

issue

8

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25 September 2017

page(s)

1206-1208

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Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

25 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

Mutations of the RET proto-oncogene in Hirschsprung's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

Novel mutations of the endothelin-B receptor gene in isolated patients with Hirschsprung's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2898%2990151-8

10.1016/S0022-3468(98)90151-8

7 January 2021

Identifiers

DOI

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25 September 2017

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