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K M Furkan Uddin Selected Research

Mucolipidosis II Alpha Beta

2/2021Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh.

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K M Furkan Uddin Research Topics

Disease

1Mucolipidosis II Alpha Beta
02/2021
146,XY Gonadal Dysgenesis (Swyer Syndrome)
02/2021
1Leigh Disease (Leigh's Disease)
02/2021
1Muscle Spasticity (Spastic)
02/2021
1Bardet-Biedl Syndrome (Syndrome, Bardet-Biedl)
02/2021

Drug/Important Bio-Agent (IBA)

1mutalipocin IIIBA
02/2021