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Ophthalmic Genet. 2017 Mar-Apr;38(2):194-196. doi: 10.1080/13816810.2016.1183217. Epub 2016 May 13.

Cutaneous freckling: Possible new clinical marker for the diagnosis of Hermansky-Pudlak syndrome in Indian Asian patients with oculocutaneous albinism.

Author information

1
a Visiting Volunteer Faculty, Pediatric Ophthalmology and Ocular Genetics , Department of Pediatric Ophthalmology and Adult Strabismus, Aravind Eye Hospital , Madurai , India.
2
b Senior Consultant and International Faculty , Pediatric Ophthalmology & Ocular Genetics, CMER (Shenzhen) Dennis Lam Hospital , Shenzhen , China.
3
c Honorary Consultant, Lumbini Eye Institute , Siddarthanagar , Nepal.
4
d Department of Genetics, Aravind Medical Research Foundation , Madurai , India.
5
e Certified Genetic Counselor , North Wales , Pennsylvania , USA.
6
f BGI-Shenzhen, Shenzhen , China.
7
g Albrecht Kossel Institute for Neuroregeneration, University of Rostock , Rostock , Germany.
8
h Centogene AG, Institute for Rare Diseases , Rostock , Germany.
9
i Constultant Dermatologist , Madurai , India.
10
j Department of Pediatric Ophthalmology and Adult Strabismus , Aravind Eye Hospital , Madurai , India.

Erratum in

PMID:
27176668
DOI:
10.1080/13816810.2016.1183217
[Indexed for MEDLINE]

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