(Q34171553)

31 July 2017

title

Challenges in whole exome sequencing: an example from hereditary deafness (English)

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31 July 2017

1 reference

Mustafa Tekin

4

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author name string

Asli Sirmaci

series ordinal

1

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31 July 2017

Yvonne J K Edwards

series ordinal

2

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31 July 2017

Hatice Akay

series ordinal

3

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31 July 2017

language of work or name

English

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publication date

21 February 2012

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31 July 2017

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31 July 2017

volume

7

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31 July 2017

issue

2

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31 July 2017

page(s)

e32000

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Creative Commons Attribution 4.0 International

31 July 2017

copyright license

start time

21 February 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Exome sequencing: a transformative technology

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Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p

5 July 2018

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Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta

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Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

5 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283682

Alanine scanning site-directed mutagenesis of the zinc fingers of transcription factor ADR1: residues that contact DNA and that transactivate

5 July 2018

1 reference

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Structure of Aart, a designed six-finger zinc finger peptide, bound to DNA.

5 July 2018

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DNA-induced α-helix capping in conserved linker sequences is a determinant of binding affinity in Cys2-His2 zinc fingers

21 January 2018

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10.1371/JOURNAL.PONE.0032000

21 January 2018

Identifiers

DOI

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31 July 2017

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31 July 2017

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