ANGELMAN SYNDROME

185 Ratings

Rs 9,720 Rs 7,200

26 % OFF

PRADER-WILLI SYNDROME (PWS) AND ANGELMAN SYNDROME (AS) ARE CLINICALLY DISTINCT NEURODEVELOPMENTAL GENETIC DISORDERS THAT MAP TO 15Q11-Q13. THE PRIMARY PHENOTYPES ARE ATTRIBUTABLE TO LOSS OF EXPRESSION OF IMPRINTED GENES WITHIN THIS REGION WHICH CAN ARISE BY MEANS OF A NUMBER OF MECHANISMS. THE MOST SENSITIVE SINGLE APPROACH TO DIAGNOSING BOTH PWS AND AS IS TO STUDY METHYLATION PATTERNS WITHIN 15Q11-Q13.

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ANGELMAN SYNDROME

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ANGELMAN SYNDROME

Rs 9,720 Rs 7,200

26 % OFF

Why book with us?

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