Literature DB >> 19406751

Three novel variants in X-linked adrenoleukodystrophy.

Pallavi Shukla1, Neerja Gupta, Madhulika Kabra, Manju Ghosh, Raju Sharma, Arun K Gupta, Sheffali Gulati, Veena Kalra.   

Abstract

X-linked adrenoleukodystrophy is an inherited neurological disorder caused by mutations in the ABCD1 gene (located on chromosome Xq28) encoding adrenoleukodystrophy protein which is involved in the transport of substrates from the cytoplasm into the peroxisomal lumen. There is a scarcity of reports on mutation analysis of X-linked adrenoleukodystrophy from India. Here, we report 3 novel variants (c.67_83del17, c.395G>A, c.1938_1939dupGG) in 3 unrelated Indian families.

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Year:  2009        PMID: 19406751     DOI: 10.1177/0883073808330764

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  3 in total

1.  Novel mutation in ATP-binding domain of ABCD1 gene in adrenoleukodystrophy.

Authors:  Neeraj Kumar; Krishna K Taneja; Atul Kumar; Deepti Nayar; Bhupesh Taneja; Satindra Aneja; Madhuri Behari; Veena Kalra; Surendra K Bansal
Journal:  J Genet       Date:  2010-12       Impact factor: 1.166

2.  Genomic profiling identifies novel mutations and SNPs in ABCD1 gene: a molecular, biochemical and clinical analysis of X-ALD cases in India.

Authors:  Neeraj Kumar; Krishna Kant Taneja; Veena Kalra; Madhuri Behari; Satinder Aneja; Surendra Kumar Bansal
Journal:  PLoS One       Date:  2011-09-22       Impact factor: 3.240

3.  A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by an unpublished mutation of ABCD1.

Authors:  Hye Jeong Jwa; Keon Su Lee; Gu Hwan Kim; Han Wook Yoo; Han Hyuk Lim
Journal:  Korean J Pediatr       Date:  2014-09-30
  3 in total

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