Publication
Lentz J, Savas S, Ng SS, Athas G, Deininger P, Keats B, The USH1C 216G-->A splice-site mutation results in a 35-base-pair deletion Human genetics116:225-7 2004 |
PubMed ID: 15578223 |
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Records Return:
(8)
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Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
GM09456 | Female | 41 YR | 2165 | mother | USHER SYNDROME, TYPE IC; USH1C | GM |
GM09459 | Male | 44 YR | 2165 | father | USHER SYNDROME, TYPE IC; USH1C | GM |
GM09458 | Male | 19 YR | 2165 | proband | USHER SYNDROME, TYPE IC; USH1C | GM |
GM09071 | Female | 12 YR | 2116 | sister | USHER SYNDROME, TYPE IC; USH1C | GM |
GM09070 | Male | 21 YR | 2116 | brother | USHER SYNDROME, TYPE IC; USH1C | GM |
GM09072 | Male | 12 YR | 2116 | brother | USHER SYNDROME, TYPE IC; USH1C | GM |
GM10359 | Male | 24 YR | 1187 | brother | USHER SYNDROME, TYPE IC; USH1C | GM |
GM10354 | Male | 21 YR | 1187 | proband | USHER SYNDROME, TYPE IC; USH1C | GM |
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