Hearing impairment: A secondary symptom in a congenital ichthyosiform erythroderma patient with ABCA12 mutations-Reference-Cited by-同舟云学术

Hearing impairment: A secondary symptom in a congenital ichthyosiform erythroderma patient with ABCA12 mutations

Author:

Murase Chiaki¹,Takeichi Takuya¹^ORCID,Sugiura Kazumitsu²,Kobayashi Miki³,Shiomi Kozue³,Ikebuchi Kaichiro⁴,Tsutsumi Yutaka⁵,Akiyama Masashi¹^ORCID

Affiliation:

1. Department of Dermatology; Nagoya University Graduate School of Medicine; Nagoya Japan

2. Department of Dermatology; Fujita Health University; Toyoake Japan

3. Department of Pediatrics; Kyoto City Hospital; Kyoto Japan

4. Department of Otolaryngology; Ikebuchi Clinic; Muko Japan

5. Division of Diagnostic Pathology; Haruhi Respiratory Medical Hospital; Kiyosu Japan

Funder

Japan Agency for Medical Research and Development

Grant-in-Aid for Scientific Research (B)

Grant-in-Aid for Young Scientists (B)

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

Reference5 articles.

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