A single mutation is responsible for the high prevalence of G6pD deficiency in the Vataliya Prajapatis—An endogamous caste group from Western India

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	American journal of hematology 2001-07, Vol.67 (3), p.218-219
Hauptverfasser:	Sukumar, Sridevi, Colah, Roshan B., Mohanty, Dipika, Joshi, Sanmukh R.
Format:	Artikel
Sprache:	eng
Schlagworte:	Codon - genetics Consanguinity Ethnic Groups - genetics Female Founder Effect Genotype Glucosephosphate Dehydrogenase - genetics Glucosephosphate Dehydrogenase Deficiency - epidemiology Glucosephosphate Dehydrogenase Deficiency - genetics Humans India - epidemiology Malaria - epidemiology Male Point Mutation Polymorphism, Genetic Selection, Genetic
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!