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ABSTRACT: Autosomal dominant gain-of-function mutations in LCP1 cause syndromic neutropenia and immunodeficiency

PROVIDER: PRJNA1247919 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR33044916.fastq.gz	Fastqsanger.gz
	SRR33044917.fastq.gz	Fastqsanger.gz
	SRR33044918.fastq.gz	Fastqsanger.gz
	SRR33044919.fastq.gz	Fastqsanger.gz
	SRR33044920.fastq.gz	Fastqsanger.gz

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