(Q34431158)

2 August 2017

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene (English)

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2 August 2017

Certain S

4

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author name string

Pastural E

1

1 reference

2 August 2017

Barrat FJ

2

1 reference

2 August 2017

Dufourcq-Lagelouse R

3

1 reference

2 August 2017

Sanal O

5

1 reference

2 August 2017

Jabado N

6

1 reference

2 August 2017

Seger R

7

1 reference

2 August 2017

Griscelli C

8

1 reference

2 August 2017

Fischer A

9

1 reference

2 August 2017

de Saint Basile G

10

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2 August 2017

language of work or name

English

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publication date

1 July 1997

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2 August 2017

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2 August 2017

16

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2 August 2017

289-292

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2 August 2017

3

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https://scigraph.springernature.com/pub.10.1038/ng0797-289

2 August 2017

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cites work

A syndrome associating partial albinism and immunodeficiency

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Partial albinism with immunodeficiency (Griscelli syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Molecular analysis of two mouse dilute locus deletion mutations: spontaneous dilute lethal20J and radiation-induced dilute prenatal lethal Aa2 alleles

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Novel myosin heavy chain encoded by murine dilute coat colour locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Unconventional Myosins

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Cloning and regional assignment of the human myosin heavy chain 12 (MYH12) gene to chromosome band 15q21.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Mapping of unconventional myosins in mouse and human

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Griscelli disease with cerebral involvement

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

A kindred with Griscelli disease: spectrum of neurological involvement

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Dilute (d) coat colour mutation of DBA/2J mice is associated with the site of integration of an ecotropic MuLV genome

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Primary structure and cellular localization of chicken brain myosin-V (p190), an unconventional myosin with calmodulin light chains

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

The Saccharomyces cerevisiae MYO2 gene encodes an essential myosin for vectorial transport of vesicles

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Identification of the homologous beige and Chediak-Higashi syndrome genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

The Chediak-Higashi Syndrome and the Homologous Trait in Animals

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Brain myosin-V is a two-headed unconventional myosin with motor activity

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Calmodulin-binding proteins as calpain substrates.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-289

7 January 2021

Identifiers

DOI

10.1038/NG0797-289

1 reference

Dimensions Publication ID

2 August 2017

0 references

1 reference