Homozygous deletion mutation of the FERMT1 gene in a Chinese patient with kindler syndrome

Seung Joon Oh, Song Ee Kim, Sang Eun Lee, SooChan Kim

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)503-505
Number of pages3
JournalAnnals of Dermatology
Volume28
Issue number4
DOIs
Publication statusPublished - 2016 Aug 1

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Sequence Deletion
Genes
Poikiloderma of Kindler

All Science Journal Classification (ASJC) codes

  • Dermatology

Cite this

Oh, Seung Joon ; Kim, Song Ee ; Lee, Sang Eun ; Kim, SooChan. / Homozygous deletion mutation of the FERMT1 gene in a Chinese patient with kindler syndrome. In: Annals of Dermatology. 2016 ; Vol. 28, No. 4. pp. 503-505.
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Homozygous deletion mutation of the FERMT1 gene in a Chinese patient with kindler syndrome. / Oh, Seung Joon; Kim, Song Ee; Lee, Sang Eun; Kim, SooChan.

In: Annals of Dermatology, Vol. 28, No. 4, 01.08.2016, p. 503-505.

Research output: Contribution to journalArticle

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