(Q30478063)

28 September 2017

Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10 (English)

1 reference

28 September 2017

1 reference

5

Roderick T Bronson

1 reference

28 September 2017

6

Muriel T Davisson

1 reference

28 September 2017

Qing Yin Zheng

1

1 reference

28 September 2017

Belinda S Harris

2

1 reference

28 September 2017

Patricia F Ward-Bailey

3

1 reference

28 September 2017

Heping Yu

4

1 reference

28 September 2017

Kenneth R Johnson

7

1 reference

28 September 2017

1 June 2004

1 reference

Academic Journal of Xi'an Jiaotong University

28 September 2017

1 reference

28 September 2017

25

1 reference

28 September 2017

3

1 reference

28 September 2017

209-212

1 reference

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004367

The original shaker-with-syndactylism mutation (sy) is a contiguous gene deletion syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004367

Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004367

Fine genetic and comparative mapping of the deafness mutation Ames waltzer on mouse chromosome 10

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004367

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004367

A type VII myosin encoded by the mouse deafness gene shaker-1

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004367

Defective myosin VIIA gene responsible for Usher syndrome type 1B

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004367

Genetic epidemiology of hearing impairment

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004367

Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locus.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004367

The Neurological Mouse Mutations Jittery and Hesitant Are Allelic and Map to the Region of Mouse Chromosome 10 Homologous to 19p13.3

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21179397

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

28 September 2017

PubMed publication ID

21179397

1 reference