Author/Creator: Govindappa, Shyla T. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Govindappa, Shyla T.

1. Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease. (March 2021)

Authors:: Kumar, Sumeet; Abbas, Masoom M.; Govindappa, Shyla T.; Muthane, Uday B.; Behari, Madhuri; Pandey, Sanjay; Juyal, Ramesh C.; Thelma, B.K.
Journal:: Parkinsonism & related disorders
Issue:: Volume 84(2021)
Page Start:: 61
Record Type:: Journal Article
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2. Early Onset Parkinson's disease due to DJ1 mutations: An Indian study. (November 2016)

Authors:: Abbas, Masoom M.; Govindappa, Shyla T.; Sudhaman, Sumedha; Thelma, B.K.; Juyal, Ramesh C.; Behari, Madhuri; Muthane, Uday B.
Journal:: Parkinsonism & related disorders
Issue:: Volume 32(2016)
Page Start:: 20
Record Type:: Journal Article
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3. Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation. Issue 1 (26th April 2016)

Authors:: Abbas, Masoom M.; Govindappa, Shyla T.; Sheerin, Una‐Marie; Bhatia, Kailash P.; Muthane, Uday B.
Journal:: Movement disorders clinical practice
Issue:: Volume 4:Issue 1(2017)
Page Start:: 132
Record Type:: Journal Article
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4. Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians. (September 2020)

Authors:: Kumar, Sumeet; Yadav, Navneesh; Pandey, Sanjay; Muthane, Uday B.; Govindappa, Shyla T.; Abbas, Masoom M.; Behari, Madhuri; Thelma, B.K.
Journal:: Parkinsonism & related disorders
Issue:: Volume 78(2020)
Page Start:: 46
Record Type:: Journal Article
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