Publication
| Hayasaka K, Himoro M, Sato W, Takada G, Uyemura K, Shimizu N, Bird TD, Conneally PM, Chance PF, Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene [see comments] Nat Genet5:31-4 1993 |
| PubMed ID: 7693129 |
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| Records Return:
(1)
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| Catalog ID | Gender | Age at Sampling | Description | Collection_Type_id |
| GM13363 | Female | 32 YR | CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B | GM |
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