SICKLE CELL ANEMIA MUTATION DETECTION

A PHP Error was encountered

Severity: 8192

Message: json_decode(): Passing null to parameter #1 ($json) of type string is deprecated

Filename: models/Product_model.php

Line Number: 247

Backtrace:

File: /home/lilj9s9ph51h/public_html/truemedix/models/Product_model.php
Line: 247
Function: json_decode

File: /home/lilj9s9ph51h/public_html/truemedix/controllers/Pages.php
Line: 138
Function: get_related

File: /home/lilj9s9ph51h/public_html/index.php
Line: 316
Function: require_once

SICKLE CELL ANEMIA MUTATION DETECTION

163 Ratings

Rs 3,930 Rs 3,000

24 % OFF

THE GENETIC DISORDER IS DUE TO THE MUTATION OF A SINGLE NUCLEOTIDE, FROM A GAG TO GTG CODON ON THE CODING STRAND. IN PEOPLE HETEROZYGOUS FOR HGBS (CARRIERS OF SICKLING HAEMOGLOBIN), THE POLYMERISATION PROBLEMS ARE MINOR, BECAUSE THE NORMAL ALLELE IS ABLE TO PRODUCE OVER 50% OF THE HAEMOGLOBIN. IN PEOPLE HOMOZYGOUS FOR HGBS, THE PRESENCE OF LONG-CHAIN POLYMERS OF HBS DISTORT THE SHAPE OF THE RED BLOOD CELL FROM A SMOOTH DOUGHNUT-LIKE SHAPE TO RAGGED AND FULL OF SPIKES, MAKING IT FRAGILE AND SUSCEPTIBLE TO BREAKING WITHIN CAPILLARIES.

Get a Free Call

To Know about Services Detail or any Enquiry.

A PHP Error was encountered