(Q47810860)

English

Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction

scientific article published on 4 August 2017

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scholarly article

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction (English)

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

Malte Spielmann

1

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

Bjørt K Kragesteen

object named as

Bjørt K Kragesteen

5

0 references

Luis R Hernandez-Miranda

object named as

Luis R Hernandez-Miranda

2

0 references

Isabella Ceccherini

object named as

Isabella Ceccherini

3

0 references

object named as

Peter Krawitz

7

0 references

10

object named as

Stefan Mundlos

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

Carmen Birchmeier

8

object named as

Carmen Birchmeier

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

author name string

Debra E Weese-Mayer

4

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

Izabela Harabula

6

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

Norma Leonard

9

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

language of work or name

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publication date

4 August 2017

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

Journal of Medical Genetics

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

54

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

11

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

754-761

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

Identifiers

10.1136/JMEDGENET-2017-104765

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

release_ub2wpe4gx5b5tnynu4afsas4im

1 reference

https://api.fatcat.wiki/v0/release/ub2wpe4gx5b5tnynu4afsas4im

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/28779001

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