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Author/Creator Krishnamoorthy, Navaneethakrishnan

3. In silico and in vivo models for Qatari‐specific classical homocystinuria as basis for development of novel therapies. Issue 2 (23rd November 2018)

Authors:
Ismail, Hesham M.; Krishnamoorthy, Navaneethakrishnan; Al‐Dewik, Nader; Zayed, Hatem; Mohamed, Nura A.; Giacomo, Valeria Di; Gupta, Sapna; Häberle, Johannes; Thöny, Beat; Blom, Henk J.; Kruger, Warren D.; Ben‐Omran, Tawfeg; Nasrallah, Gheyath K.
Journal:
Human mutation
Issue:
Volume 40:Issue 2(2019)
Page Start:
230
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss. (January 2019)

Authors:
Morgan, Anna; Vuckovic, Dragana; Krishnamoorthy, Navaneethakrishnan; Rubinato, Elisa; Ambrosetti, Umberto; Castorina, Pierangela; Franzè, Annamaria; Vozzi, Diego; La Bianca, Martina; Cappellani, Stefania; Di Stazio, Mariateresa; Gasparini, Paolo; Girotto, Giorgia
Journal:
European journal of human genetics
Issue:
Volume 27:Number 1(2019)
Page Start:
70
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗