A new nonsense mutation in HMX1 in two siblings with oculoauricular syndrome. (3rd September 2022)
- Record Type:
- Journal Article
- Title:
- A new nonsense mutation in HMX1 in two siblings with oculoauricular syndrome. (3rd September 2022)
- Main Title:
- A new nonsense mutation in HMX1 in two siblings with oculoauricular syndrome
- Authors:
- Ansar, Muhammad
Javed, Samra
Baig, Hafiz Muhammad Azhar
Quinodoz, Mathieu
Ullah, Mukhtar
Han, Ji Hoon
Rahim, Muhammad Usama
Kausar, Humera
Calzetti, Giacomo
Rivolta, Carlo - Abstract:
- Is Part Of:
- Ophthalmic genetics. Volume 43:Number 5(2022)
- Journal:
- Ophthalmic genetics
- Issue:
- Volume 43:Number 5(2022)
- Issue Display:
- Volume 43, Issue 5 (2022)
- Year:
- 2022
- Volume:
- 43
- Issue:
- 5
- Issue Sort Value:
- 2022-0043-0005-0000
- Page Start:
- 720
- Page End:
- 723
- Publication Date:
- 2022-09-03
- Subjects:
- Eye -- Diseases -- Genetic aspects -- Periodicals
Eye Diseases -- genetics -- Periodicals
Eye Diseases -- in infancy & childhood -- Periodicals
617.7 - Journal URLs:
- http://informahealthcare.com/loi/opg ↗
http://informahealthcare.com ↗
http://www.tandf.co.uk/journals/titles/13816810.asp ↗ - DOI:
- 10.1080/13816810.2022.2096242 ↗
- Languages:
- English
- ISSNs:
- 1381-6810
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6270.893000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 23950.xml