A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases.
about
Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding.High-throughput sequencing for rapid diagnosis of inherited platelet disorders: a case for a European consensus.Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.
P2860
A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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name
A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases.
@en
type
label
A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases.
@en
prefLabel
A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases.
@en
P2093
P2860
P1476
A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases.
@en
P2093
Daniel Greene
NIHR BioResource
Sylvia Richardson
P2860
P304
P356
10.1016/J.AJHG.2017.05.015
P407
P50
P577
2017-06-27T00:00:00Z