PRADERWILLI SYNDROME MARKET AARKSTORE ENTERPRISE
Uptill 3rd Aug, 2018
+91 9987295242 contact@aarkstore.comÂ
REPORT STUDY
In the majority of cases, there is a deletion. In remaining cases, the entire chromosome from the father is missing and there are instead two chromosome 15s from the mother (uniparental disomy).
Prader-Willi Syndrome market, provides an overview of the Prader-Willi Syndrome (PWS) (Genetic Disorders) pipeline landscape. Prader-Willi Syndrome (PWS) is a rare genetic disorder present at birth that results in a number of physical, mental and behavioral problems. PWS is due to lack of several genes on one of an individuals two chromosome 15s.
+91 9987295242contact@aarkstore.com
KEY HIGHLIGHTS
SYMPTOMS
Muscle tone Low levels of sex hormones A constant feeling of hunger.Â
Therapeutics under Development by Companies /Universities /Institutes The molecules developed by Companies in Phase III, Phase II Phase I, IND/CTA Filed Preclinical and Discovery stages are 3, 6, 3, 1, 3 and 1 respectivelyÂ
Prader-Willi Syndrome Market Research Report 2018
+91 9987295242contact@aarkstore.com
SCOPE Snapshot of the global therapeutic landscape of Prader-Willi Syndrome (PWS) Companies and universities/research institutes based on information derived from company and industry-specific sources Covers pipeline products based on several stages of development
Healthcare Market Research Reports
Comprise, product description, descriptive licensing and collaboration details Encapsulates all the dormant and discontinued pipeline projects
+91 9987295242contact@aarkstore.com
19
RELATED REPORTS
Prader-Willi Syndrome (PWS) Global Clinical Trials Review, H1, 2018 Prader-Willi Syndrome (PWS) Global Clinical Trials Review, H1, 2018 Global Prader-Willi Syndrome (PWS) Market Research Report 2018 CHECK THE DISCOUNT HERE -
https://www.aarkstore.com/discount.php
+91 9987295242contact@aarkstore.com