Zobrazeno 1 - 3
of 3
pro vyhledávání: '"member a1 gene"'
Autor:
Sangeetha Yoganathan, Gautham Arunachal, Lisa Kratz, Mugil Varman, Maya Thomas, Sniya Valsa Sudhakar, Samuel Philip Oommen, Sumita Danda
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 1, Pp 113-117 (2020)
Succinic semialdehyde dehydrogenase (SSADH) deficiency is an autosomal recessive disorder of gamma-aminobutyric acid metabolism. Children with SSADH deficiency usually manifest with developmental delay, behavioral symptoms, language dysfunction, seiz
Externí odkaz:
https://doaj.org/article/4b12d668aa3648e6bd2ea4ba1dd4dbb3
Autor:
Sumita Danda, Mugil Varman, Sniya Valsa Sudhakar, Lisa E. Kratz, Gautham Arunachal, Samuel Philip Oommen, Sangeetha Yoganathan, Maya Thomas
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 1, Pp 113-117 (2020)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
Succinic semialdehyde dehydrogenase (SSADH) deficiency is an autosomal recessive disorder of gamma-aminobutyric acid metabolism. Children with SSADH deficiency usually manifest with developmental delay, behavioral symptoms, language dysfunction, seiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::946ec9f1129d7915ed3a1a8b60b947dd
http://www.annalsofian.org/article.asp?issn=0972-2327
http://www.annalsofian.org/article.asp?issn=0972-2327
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