Increasing the complexity: new genes and new types of albinism-Reference-Cited by-同舟云学术

Increasing the complexity: new genes and new types of albinism

Published:2013-10-17 Issue:1 Volume:27 Page:11-18
ISSN:1755-1471
Container-title:Pigment Cell & Melanoma Research
language:en
Short-container-title:Pigment Cell Melanoma Res

Author:

Montoliu Lluís¹²,Grønskov Karen³⁴,Wei Ai-Hua⁵,Martínez-García Mónica¹²,Fernández Almudena¹²,Arveiler Benoît⁶⁷,Morice-Picard Fanny⁶⁷,Riazuddin Saima⁸⁹,Suzuki Tamio¹⁰,Ahmed Zubair M.⁸⁹,Rosenberg Thomas¹¹¹²,Li Wei¹³

Affiliation:

1. Department of Molecular and Cellular Biology; National Centre for Biotechnology (CNB-CSIC); Campus de Cantoblanco; Madrid Spain

2. CIBERER, ISCIII; Madrid Spain

3. Applied Human Molecular Genetics; Kennedy Center; Copenhagen University Hospital; Copenhagen Denmark

4. Department of Cellular and Molecular Medicine; University of Copenhagen; Copenhagen Denmark

5. Department of Dermatology; Beijing Tongren Affiliated Hospital of Capital Medical University; Beijing China

6. Maladies Rares: Génétique et Métabolisme (MRGM) EA4576; Univ. Bordeaux; Bordeaux France

7. Service de Génétique Médicale; CHU de Bordeaux; Bordeaux France

8. Divisions of Pediatric Ophthalmology and Otolaryngology; Cincinnati Children's Hospital Research Foundation; Cincinnati OH USA

9. Departments of Ophthalmology and Otolaryngology; University of Cincinnati; Cincinnati OH USA

10. Department of Dermatology; Faculty of Medicine; Yamagata University; Yamagata Japan

11. National Eye Clinic for the Visually Impaired; Kennedy Center; Copenhagen University Hospital; Copenhagen Denmark

12. Institute of Clinical Medicine; Faculty of Health; University of Copenhagen; Copenhagen Denmark

13. State Key Laboratory of Molecular Developmental Biology; Institute of Genetics and Developmental Biology; Chinese Academy of Sciences; Beijing China

Publisher

Wiley

Subject

Dermatology,General Biochemistry, Genetics and Molecular Biology,Oncology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pcmr.12167/fullpdf

Reference67 articles.

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5. BLOC-1 mutation screen reveals that PLDN is mutated in Hermansky-Pudlak syndrome type 9;Cullinane;Am. J. Hum. Genet.,2011

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