Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects-Reference-Cited by-同舟云学术

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Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects

Published:2019-02-28 Issue:10 Volume:104 Page:2084-2090
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Gorski Marcin M.,Lecchi Anna,Femia Eti A.,La Marca Silvia,Cairo Andrea,Pappalardo Emanuela,Lotta Luca A.,Artoni Andrea,Peyvandi Flora

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Roles of G proteins and their GTPase-activating proteins in platelets;Bioscience Reports;2024-05

2. Flow-chamber device (T-TAS) to diagnose patients suspected of platelet function defects;BLOOD TRANSFUS-ITALY;2024

3. Diverse targets of SMN2-directed splicing-modulating small molecule therapeutics for spinal muscular atrophy;Nucleic Acids Research;2023-04-07

4. A Missense Variation in PHACTR2 Associates with Impaired Actin Dynamics, Dilated Cardiomyopathy, and Left Ventricular Non-Compaction in Humans;International Journal of Molecular Sciences;2023-01-10

5. Missense mutations in inositol 1,4,5-trisphosphate receptor type 3 result in leaky Ca2+ channels and activation of store-operated Ca2+ entry;iScience;2022-12

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