A second, large deletion in the HEXB gene in a patient with infantile Sandhoff disease

Journal Article A second, large deletion in the HEXB gene in a patient with infantile Sandhoff disease Get access Zhi-Xin Zhang, Zhi-Xin Zhang Search for other works by this author on: Oxford Academic PubMed Google Scholar Nobuaki Wakamatsu, Nobuaki Wakamatsu Search for other works by this author on: Oxford Academic PubMed Google Scholar Beverly R. Akerman, Beverly R. Akerman Search for other works by this author on: Oxford Academic PubMed Google Scholar Emily H. Mules, Emily H. Mules 1Center for Advanced Biotechnology and Medicine, Rutgers UniversityRutgers, NJ, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar George H. Thomas, George H. Thomas 2Genetics Laboratory, The Kennedy InstituteBaltimore, MD, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Roy A. Gravel Roy A. Gravel * *To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 4, Issue 4, April 1995, Pages 777–780, https://doi.org/10.1093/hmg/4.4.777 Published: 01 April 1995 Article history Received: 20 January 1995 Revision received: 31 January 1995 Accepted: 31 January 1995 Published: 01 April 1995