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A new sequence motif linking lissencephaly, Treacher Collins and oral-facial-digital type 1 syndromes, microtubule dynamics and cell migration.

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...

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Publisher copy:
10.1093/hmg/10.24.2813

Authors


Ponting, CP More by this author
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

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