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Year : 2021 | Volume: 16 | Issue Number: 2 | Page: 153-155 CASE REPORTRapidly progressive spastic paraplegia due to hyperhomocysteinemia in child with MTHFR gene mutation and mitochondrial Complex I deficiency: A rare association Mahale Rohan R, Gautam Jyothi, Arunachal Gautam, Alappati Sandhya, Varghese Nibu, Kovoor Jennifer, Mailankody Pooja, Padmanabha Hansashree, Pavagada Mathuranath
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