An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis

✍ Scribed by Nancy S Elbarbary; Erling Tjora; Janne Molnes; Benedicte A Lie; Mohammad A Habib; Mona A Salem; Pål Rasmus Njølstad

• Book ID: 117948439
• Publisher: John Wiley and Sons
• Year: 2012
• Tongue: English
• Weight: 594 KB
• Volume: 14
• Category: Article
• ISSN: 1399-543X
• DOI: 10.1111/j.1399-5448.2012.00925.x