Family NIGMS00069 Members
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Records Return:
(2)
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Catalog ID | Description | Sex | Age | Race | Affected | Family Member | Relationship to Proband | Cell Type | Family |
GM28774 | CEREBRAL CREATINE DEFICIENCY SYNDROME 1; CCDS1 | Male | 10 YR | White | Yes | 1 | proband | B-Lymphocyte | NIGMS00069 |
GM28876 | CEREBRAL CREATINE DEFICIENCY SYNDROME 1; CCDS1 | Male | 10 YR | White | Yes | 1 | proband | Fibroblast | NIGMS00069 |
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