Duchenne muscular dystrophy: A clinical, histopathological and genetic study at a neurology tertiary care center in southern India

Emery, 1998, BMJ, The Muscular Dystrophies, 991

Tennyson, 1995, Nat Genet, The human dystrophin gene requires 16 h to be transcribed and is cotranscriptionally spliced, 184

Hoffman EP, Brown RH Jr, Kunkel LM. Dystrophin: The protein product of the Duchenne muscular dystrophy locus. Cell 1987;51:919-28.

Forrest, 1987, Nature, Preferential deletion of exons in Duchenne and Becker muscular dystrophies, 638

Forrest, 1988, Genomics, Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies, 109

Koenig, 1987, Cell, Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals, 509

Koenig, 1989, Am J Hum Genet, The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion, 498

Beggs, 1990, Hum Genet, Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction, 45

Engel AG. Duchenne Dystrophy. In: Engel AG, Banker BQ, editors Myology: Basic and clinical. Vol. 2. New York: Mc Graw-Hill; 1986. p. 1185-240.

Kamat VV. Measuring intelligence of Indian children. 4 th ed. Bombay: Oxford University Press; 1967.

Miller, 1988, Nucleic Acids Res, A simple salting out procedure for extracting DNA from human nucleated cells, 1215

Chamberlain, 1988, Nucleic Acids Res, Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification, 11141

Purushottam, 2008, J Neurol Sci, Paternal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India, 179

Dubowitz V. Muscle disorders in childhood. Major problems in clinical pediatrics. London: Saunders Co. Ltd; 1978.

Walton J N and Gardner-Medwin D. In: Walton SJ, editor. Disorders of Voluntary Muscle. Edinburgh: Churchill Livingstone; 1981. p. 481-524.

Lebart. Multivariate descriptive statistical methods: Correspondence analysis and related techniques. New York: Wileey; 1984.

Feingold, 1971, Ann Genet, Genes majeurs, genes modificateurs et effets du milieu dans la myopathie de duchenne de Boulogne, 207

Brooke, 1989, Neurology, Duchenne muscular dystrophy: Patterns of clinical progression and effects of supportive therapy, 475

Furukawa, 1977, Ann Neurol, X-linked muscular dystrophy, 414

Lindlöf, 1989, Am J Hum Genet, Gene deletions in X-linked muscular dystrophy, 496

Hodgson, 1992, Neuromuscul Disord, Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability, 269

Ballo, 1994, S Afr Med J, Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected, 494

Bresolin, 1994, Neuromuscul Disord, Cognitive impairment in Duchenne muscular dystrophy, 359

Odinokova, 1996, Genetika, Deletion analysis of the dystrophin gene in patients with Duchenne′s muscular dystrophy in Tajikistan, 1392

Singh, 1997, Hum Genet, Proportion and pattern of dystrophin gene deletions in north Indian Duchenne and Becker muscular dystrophy patients, 206

Haider, 1998, Human Hered, Screening 25 dystrophin gene exons for deletions in Arab children with Duchenne muscular dystrophy, 61

Hoffman, 1989, Neurology, Improved diagnosis of Becker muscular dystrophy by dystrophin testing, 1011

Dubowitz V. Muscle disorders in Childhood. London: Saunders; 1995.

Banerjee, 1997, Am J Med Genet, Are there ethnic differences in the dystrophin gene?, 152

Basak, 2006, Neurology India, Analysis of dystrophin gene deletions by multiplex PCR in eastern India, 310

Mallikarjuna, 2003, Indian J Med Sci, Dystrophin gene deletions in South Indian Duchenne muscular dystrophy patients, 1

Khalap, 1997, Indian J Hum Genet, A report on higher frequency of DMD gene deletion in the Indian subcontinent, 117

Nadkarni, 2008, Neurol India, Duchenne and Becker muscular dystrophies: An Indian update on genetics and rehabilitation, 248

Hassan, 2008, Pediatr Int, Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients, 162

Wang, 2008, Behav Brain Funct, Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations, 4:20