Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2261

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease ; volume:18 ; number:1 ; day:3 ; month:7 ; year:2018 ; pages:1-7 ; date:12.2018
BMC cardiovascular disorders ; 18, Heft 1 (3.7.2018), 1-7, 12.2018

Creator: Razmara, Ehsan

Contributor: Garshasbi, Masoud
SpringerLink (Online service)

DOI: 10.1186/s12872-018-0867-4

URN: urn:nbn:de:101:1-2018090322232937509370

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:21 AM CEST

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Razmara, Ehsan
Garshasbi, Masoud
SpringerLink (Online service)

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Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease

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Other Objects (12)

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera

Whole-exome sequencing of a pedigree segregating asthma

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma

Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss

Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population

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Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera

Whole-exome sequencing of a pedigree segregating asthma

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia

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Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma

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