Duygu Duman Selected Research

type 3 Stickler syndrome

8/2015

Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53.

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Duygu Duman Research Topics

Disease

4	Deafness (Deaf Mutism) 10/2019 - 09/2014
2	Sensorineural Hearing Loss 01/2019 - 11/2012
2	Hearing Loss (Hearing Impairment) 01/2012 - 05/2010
1	Stroke (Strokes) 01/2022
1	Lactic Acidosis 01/2022
1	Mitochondrial Diseases (Mitochondrial Disease) 01/2022
1	Leigh Disease (Leigh's Disease) 01/2022
1	MERRF Syndrome (Myoclonic Epilepsy and Ragged Red Fibers) 01/2022
1	Mitochondrial encephalopathy 01/2022
1	Optic Nerve Diseases (Optic Neuropathy) 01/2022
1	Nonsyndromic Deafness 01/2022
1	Branchio-Oto-Renal Syndrome (Branchio Oculo Facial Syndrome) 07/2017
1	Pierre Robin syndrome with fetal chondrodysplasia 08/2015
1	type 3 Stickler syndrome 08/2015
1	Megaepiphyseal dwarfism 08/2015

Drug/Important Bio-Agent (IBA)

4	DNA (Deoxyribonucleic Acid)IBA 01/2022 - 01/2016
3	Proteins (Proteins, Gene)FDA Link 01/2019 - 05/2010
1	Mitochondrial DNA (mtDNA)IBA 01/2022
1	Tight Junction ProteinsIBA 10/2019
1	ClaudinsIBA 10/2019
1	Receptor Tyrosine Kinase-like Orphan ReceptorsIBA 05/2016
1	Collagen Type XIIBA 08/2015
1	NucleotidesIBA 09/2014
1	MorpholinosIBA 11/2012
1	Connexin 26IBA 01/2012
1	Messenger RNA (mRNA)IBA 05/2010