Improved molecular diagnosis of the common recurrent intragenic deletion mutation inIKBKGin a Filipino family with incontinentia pigmenti-Reference-Cited by-同舟云学术

Improved molecular diagnosis of the common recurrent intragenic deletion mutation inIKBKGin a Filipino family with incontinentia pigmenti

Author:

Guevara Bryan Edgar K¹,Hsu Chao-Kai²³⁴,Liu Lu⁵,Feast Alice²,Alabado Karen Lee P¹,Lacuesta Maricarr Pamela M¹,Lee Julia Yu-Yun³,McGrath John A²

Affiliation:

1. Department of Dermatology; Southern Philippines Medical Center; Davao Philippines

2. St John's Institute of Dermatology; King's College London; London UK

3. Department of Dermatology; National Cheng Kung University Hospital; Tainan Taiwan

4. Institute of Clinical Medicine; College of Medicine; National Cheng Kung University; Tainan Taiwan

5. Viapath; St Thomas' Hospital; London UK

Funder

National Institute for Health Research

Guy's and St Thomas' National Health Service Foundation Trust

King’s College London

Publisher

Wiley

Subject

Dermatology

Link

Reference10 articles.

1. Incontinentia pigmenti (Bloch-Sulzberger syndrome): a systemic disorder;Ehrenreich;Cutis,2007

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