Association of MITF gene with hearing and pigmentation phenotype in Hedlund white American mink (Neovison vison). (Q50354387)

6 March 2018

title

Association of MITF gene with hearing and pigmentation phenotype in Hedlund white American mink (Neovison vison). (English)

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6 March 2018

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5

Razvan Anistoroaei

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6 March 2018

author name string

Marios N Markakis

1

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6 March 2018

Vibeke E Soedring

2

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6 March 2018

Vibeke Dantzer

3

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6 March 2018

Knud Christensen

4

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6 March 2018

publication date

1 August 2014

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6 March 2018

published in

Journal of Genetics

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6 March 2018

volume

93

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6 March 2018

issue

2

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6 March 2018

page(s)

477-481

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6 March 2018

Albinism in the American mink (Neovison vison) is associated with a tyrosinase nonsense mutation

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A MITF mutation associated with a dominant white phenotype and bilateral deafness in German Fleckvieh cattle

21 January 2018

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A role of the microphthalmia-associated transcription factor in congenital sensorineural deafness and eye pigmentation in Dalmatian dogs

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Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics

21 January 2018

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Pigmented cells of the stria vascularis and spiral ligament of the chinchilla

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Comparative anatomy of melanin pigment in the stria vascularis. Evidence for a distinction between melanocytes and intermediate cells in the cat

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12 December 2020

Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner ear.

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Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material

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Mutation in intron 6 of the hamster Mitf gene leads to skipping of the subsequent exon and creates a novel animal model for the human Waardenburg syndrome type II.

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Identifiers

DOI

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6 March 2018

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6 March 2018