- Abstract:
-
A previously unidentified sequence motif has been identified in the products of genes mutated in Miller-Dieker lissencephaly, Treacher Collins, oral-facial-digital type 1 and contiguous syndrome ocular albinism with late onset sensorineural deafness syndromes. An additional homologous motif was detected in a gene product fused to the fibroblast growth factor receptor type 1 in patients with an atypical stem cell myeloproliferative disorder. In total, over 100 eukaryotic intracellular proteins...
Expand abstract - Publisher copy:
- 10.1093/hmg/10.24.2813
-
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- Journal:
- Human molecular genetics
- Volume:
- 10
- Issue:
- 24
- Pages:
- 2813-2820
- Publication date:
- 2001-11-05
- DOI:
- EISSN:
-
1460-2083
- ISSN:
-
0964-6906
- URN:
-
uuid:988b1a82-1c7a-4228-8b3f-b47a92820edc
- Source identifiers:
-
238077
- Local pid:
- pubs:238077
- Language:
- English
- Keywords:
- Copyright date:
- 2001
Journal article
A new sequence motif linking lissencephaly, Treacher Collins and oral-facial-digital type 1 syndromes, microtubule dynamics and cell migration.
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