Identification of a novel compound heterozygous mutation in BBS12 in an Iranian family with bardet-biedl syndrome using targeted next generation sequencing
Cell Journal [Yakhteh]. 2018; 20 (2): 284-289
in En
| IMEMR
| ID: emr-198741
Responsible library:
EMRO
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Index:
IMEMR
Language:
En
Journal:
Cell J. [Yakhteh]
Year:
2018