Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India-Reference-Cited by-同舟云学术

Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India

Published:2020-03-24 Issue:9 Volume:39 Page:2743-2749
ISSN:0770-3198
Container-title:Clinical Rheumatology
language:en
Short-container-title:Clin Rheumatol

Author:

Danda Sumita,Mohan Sony,Devaraj Prabavathi,Dutta Atanu K.,Nampoothiri Sheela,Yesodharan Dhanya,Phadke Shubha R.,Jalan Anil B.,Thangaraj K.,Verma Ishwar Chandra,Danda Debashish,Jebaraj Isaac

Funder

Indian Council of Medical Research

Christian Medical College, Vellore

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Rheumatology

Link

http://link.springer.com/content/pdf/10.1007/s10067-020-05020-8.pdf

Reference19 articles.

1. Phornphutkul C, Introne WJ, Perry MB, Bernardini I, Murphey MD, Fitzpatrick DL, Anderson PD, Huizing M, Anikster Y, Gerber LH, Gahl WA (2002) Natural history of alkaptonuria. N Engl J Med 347:2111–2121

2. Vilboux T, Kayser M, Introne WJ, Suwannarat P, Bernardini I, Fischer R et al (2009) Mutation spectrum of homogentisic acid oxidase (HGD) in alkaptonuria. Hum Mutat 30:1611–1619