Zobrazeno 1 - 2
of 2
pro vyhledávání: '"PE Sonylal"'
Publikováno v:
Journal of Dr. NTR University of Health Sciences, Vol 5, Iss 1, Pp 55-58 (2016)
Alkaptonuria (AKU) is a rare autosomal recessive disorder caused by deficiency of homogentisate 1,2-dioxygenase, an enzyme that converts homogentisic acid (HGA) to maleylacetoacetic acid in the tyrosine degradation pathway. The three major features o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb39421d225cfd37266fe584b8316010
http://www.jdrntruhs.org/article.asp?issn=2277-8632
http://www.jdrntruhs.org/article.asp?issn=2277-8632
Autor:
Rao MS; Associate Professor, Department of Otorhinolaryngology and Head and Neck Surgery, Dr Pinnamaneni Siddhartha Institute of Medical Sciences and Research Foundation , Chinnaoutpalli,Gannavaram Mandal, Krishna District, Andhra Pradesh, India ., Lakshmi CR; Assistant Professor, Department of Oral Medicine and Radiology, Drs Sudha and Nageswara Rao Siddhartha Institute of Dental Sciences , Chinnaoutpalli, Gannavaram Mandal, Krishna District, Andhra Pradesh, India ., Sonylal PE; Associate Professor, Department of Neurosurgery, Associate Professor, Dr Pinnamaneni Siddhartha Institute of Medical Sciences and Research Foundation , Chinnaoutpalli, Gannavaram Mandal, Krishna District, Andhra Pradesh, India ., Chakravarthy VK; Associate Professor, Department of General Pathology, Dr Pinnamaneni Siddhartha Institute of Medical Sciences and Research Foundation , Chinnaoutpalli, Gannavaram Mandal, Krishna District, Andhra Pradesh, India ., Murthy PS; Professor & Head of the Department, Department of Otorhinolaryngology and Head and Neck Surgery, Dr Pinnamaneni Siddhartha Institute of Medical Sciences and Research Foundation , Chinnaoutpalli, Gannavaram Mandal, Krishna District, Andhra Pradesh, India .
Publikováno v:
Journal of clinical and diagnostic research : JCDR [J Clin Diagn Res] 2014 Jun; Vol. 8 (6), pp. KD01-2. Date of Electronic Publication: 2014 Jun 20.