Gaurav V Harlalka
3PUBLICATIONS
30CO-AUTHORS
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Publications (3)
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|Jun 21, 2022
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.Guney Bademci, María Lachgar-Ruiz, Mangesh Deokar
|Mar 17, 2022
Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice.Lettie E Rawlins, Hashem Almousa, Shazia Khan
|Jan 14, 2022
Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B).Siying Lin, Aida Sanchez-Bretaño, Joseph S Leslie
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Frequent Collaborators
2 joint publications
Emma L Baple
1 joint publications
Guney Bademci
1 joint publications
María Lachgar-Ruiz
1 joint publications
Mohammad Faraz Zafeer
1 joint publications
Clemer Abad
1 joint publications
Neil J Ingham
1 joint publications
Ioannis Karakikes
1 joint publications
Duygu Duman
1 joint publications
Barry A Chioza
1 joint publications
Karen P Steel
