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MAA microphthalmia or anophthalmia and associated anomalies [Homo sapiens (human)]

Gene Symbol MAA
Entrez Gene ID 4080
Full Name microphthalmia or anophthalmia and associated anomalies
Synonyms LZMS, MCOPS1
General protein information
Gene Type unknown
Organism Homo sapiens (human)
Genome

X

Summary lac of sum
Disorder MIM:

309800

Disorder Html: Microphthalmia, syndromic 1 (2)
CloneID RefSeq Accession Definition **Vector *Turnaround time Price

*Business Day
**You may select a custom vector to replace pcDNA3.1-C-(k)DYK after clone is added to cart.