Leena Shingavi

A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patients

H. Lochmüller, R. Horvath, M. Faruq, 2021, neurogenetics.

Altered REM sleep architecture in patients with Myotonic dystrophy type 1: is related to sleep apnea?

A. Nalini, R. Yadav, K. Polavarapu, 2021, Sleep medicine.

Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

I. Nishino, R. Horvath, D. Nagabushana, 2021, Journal of Human Genetics.

Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

I. Nishino, R. Horvath, A. Nalini, 2021, Journal of Human Genetics.

Social Cognition Deficits Are Pervasive across Both Classical and Overlap Frontotemporal Dementia Syndromes

A. Nalini, P. Pal, S. Alladi, 2020, Dementia and Geriatric Cognitive Disorders Extra.