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Marie-Louise Lovgren Selected Research

Vohwinkel syndrome

10/2020A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies.

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Marie-Louise Lovgren Research Topics

Disease

1Vohwinkel syndrome
10/2020
1Deafness (Deaf Mutism)
10/2020
1Ichthyosis (Xeroderma)
10/2020
1Keratitis
10/2020
1Hearing Loss (Hearing Impairment)
10/2020
1Channelopathies
10/2020
1Mycosis Fungoides
02/2019

Drug/Important Bio-Agent (IBA)

1Connexin 26IBA
10/2020
1ConnexinsIBA
10/2020
1Connexin 43 (Connexin43)IBA
10/2020

Therapy/Procedure

1Therapeutics
02/2019