Literature DB >> 21328435

Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: compound heterozygous for NADH-cytochrome b5 reductase gene mutations.

Prabhakar S Kedar1, Prashant Warang, Kanjaksha Ghosh, Roshan B Colah.   

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Year:  2011        PMID： 21328435     DOI： 10.1002/ajh.21956

Source DB:  PubMed          Journal:  Am J Hematol        ISSN： 0361-8609            Impact factor:   10.047


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  3 in total

1.  A novel nine base deletion mutation in NADH-cytochrome b5 reductase gene in an Indian family with recessive congenital methemoglobinemia-type-II.

Authors:  Prashant Warang; Prabhakar Kedar; S Sivanandam; K Jothilakshmi; R Sumathi; Roshan Colah
Journal:  Mol Genet Metab Rep       Date:  2015-10-22

2.  Neurological and Neuroimaging Features of CYB5R3-Related Recessive Hereditary Methemoglobinemia Type II.

Authors:  Francesco Nicita; Letizia Sabatini; Viola Alesi; Giulia Lucignani; Ester Sallicandro; Antonella Sferra; Enrico Bertini; Ginevra Zanni; Giuseppe Palumbo
Journal:  Brain Sci       Date:  2022-01-29

3.  Congenital methemoglobinemia type II in a 5-year-old boy.

Authors:  Elizabeth A Mannino; Thomas Pluim; Jacob Wessler; Megan T Cho; Jane Juusola; Samantha A Schrier Vergano
Journal:  Clin Case Rep       Date:  2017-12-07
  3 in total

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