Publication
Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2d, Nikoskelainen EK, Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science242:1427-30 1988 |
PubMed ID: 3201231 |
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Records Return:
(4)
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Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
GM03857 | Male | 33 YR | 567 | proband | CONGENITAL OPTIC ATROPHY, TYPE UNKNOWN | GM |
GM03858 | Male | 33 YR | 567 | proband | CONGENITAL OPTIC ATROPHY, TYPE UNKNOWN | GM |
GM10744 | Male | 53 YR | 1252 | proband | LEBER OPTIC ATROPHY | GM |
GM10742 | Male | 30 YR | | proband | LEBER OPTIC ATROPHY | GM |
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