Unusual dermatological presentation and immune phenotype in SCID due to an IL7R mutation: the value of whole-exome sequencing and the potential benefit of newborn screening


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Date

2017-03

Publication Type

Other Journal Item

ETH Bibliography

no

Citations

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Data

Rights / License

Publication status

published

Editor

Book title

Volume

31 (3)

Pages / Article No.

Publisher

Wiley-Blackwell

Event

Edition / version

Methods

Software

Geographic location

Date collected

Date created

Subject

Organisational unit

02207 - Functional Genomics Center Zurich / Functional Genomics Center Zurich check_circle

Notes

Funding

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