2 results for author:"Mimouni-Bloch A." in Literature citations
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| Infantile cerebral and cerebellar atrophy is associated with a mutation in the MED17 subunit of the transcription preinitiation mediator complex. Kaufmann R., Straussberg R., Mandel H., Fattal-Valevski A., Ben-Zeev B., Naamati A., Shaag A., Zenvirt S., Konen O., Mimouni-Bloch A. et al. Am. J. Hum. Genet. 87:667-670(2010) · UniProtKB (1) · Mapped (2) |
| Late infantile neuronal ceroid lipofuscinosis: a new mutation in Arabs. Goldberg-Stern H., Halevi A., Marom D., Straussberg R., Mimouni-Bloch A. Pediatr. Neurol. 41:297-300(2009) · Mapped (10) |