(PDF) Correction: Whole-Exome Sequencing Identifies a Novel

Correction: Whole-Exome Sequencing Identifies a Novel CCDC151 Mutation, C.325GT (p.E109X), in a Patient With Primary Ciliary Dyskinesia and Situs Inversus

Journal of Human Genetics - United Kingdom

doi 10.1038/s10038-019-0624-2

Full Text

Open PDF

Abstract

Available in full text

Date

June 10, 2019

Authors

Publisher

Springer Science and Business Media LLC

Related search

A Rare Cause of Acute Abdominal Pain in a Patient With Primary Ciliary Dyskinesia With Situs Inversus Totalis

Turkish Journal of Pediatrics

English

Whole Exome Sequencing Identifies a Novel Dominant Missense Mutation Underlying Leukonychia in a Pakistani Family

Journal of Human Genetics

Genetics

2018

English

Whole Exome Sequencing Identifies a Novel and a Recurrent Mutation inBBS2Gene in a Family With Bardet-Biedl Syndrome

BioMed Research International

English

Whole-Exome Sequencing Identifies a Potential TTN Mutation in a Multiplex Family With Inguinal Hernia

Hernia : the journal of hernias and abdominal wall surgery

Surgery

2016

English

Whole‑exome Sequencing Identifies a Novel Mutation (R367G) in SCN5A to Be Associated With Familial Cardiac Conduction Disease

Molecular Medicine Reports

English

Whole Exome Sequencing Identifies a Novel Hedgehog-Interacting Protein G516R Mutation in Locally Advanced Papillary Thyroid Cancer

International Journal of Molecular Sciences

Organic Chemistry

Molecular Biology

Theoretical Chemistry

Inorganic Chemistry

Computer Science Applications

English

Exome Sequencing Identifies a Novel MAP3K14 Mutation in Recessive Atypical Combined Immunodeficiency

Frontiers in Immunology

Allergy

Immunology

2017

English

Exome Sequencing Identifies a Novel SMCHD1 Mutation in Facioscapulohumeral Muscular Dystrophy 2

Neuromuscular Disorders

English

Clinical Exome Sequencing Identifies a Novel TUBB4A Mutation in a Child With Static Hypomyelinating Leukodystrophy

Pediatric Neurology

Child Health

Developmental Neuroscience

English

Amanote Research

Correction: Whole-Exome Sequencing Identifies a Novel CCDC151 Mutation, C.325GT (p.E109X), in a Patient With Primary Ciliary Dyskinesia and Situs Inversus

Journal of Human Genetics - United Kingdom

doi 10.1038/s10038-019-0624-2

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

A Rare Cause of Acute Abdominal Pain in a Patient With Primary Ciliary Dyskinesia With Situs Inversus Totalis

Whole Exome Sequencing Identifies a Novel Dominant Missense Mutation Underlying Leukonychia in a Pakistani Family

Whole Exome Sequencing Identifies a Novel and a Recurrent Mutation inBBS2Gene in a Family With Bardet-Biedl Syndrome

Whole-Exome Sequencing Identifies a Potential TTN Mutation in a Multiplex Family With Inguinal Hernia

Whole‑exome Sequencing Identifies a Novel Mutation (R367G) in SCN5A to Be Associated With Familial Cardiac Conduction Disease

Whole Exome Sequencing Identifies a Novel Hedgehog-Interacting Protein G516R Mutation in Locally Advanced Papillary Thyroid Cancer

Exome Sequencing Identifies a Novel MAP3K14 Mutation in Recessive Atypical Combined Immunodeficiency

Exome Sequencing Identifies a Novel SMCHD1 Mutation in Facioscapulohumeral Muscular Dystrophy 2

Clinical Exome Sequencing Identifies a Novel TUBB4A Mutation in a Child With Static Hypomyelinating Leukodystrophy