Gene: [16p12/RP22] retinitis pigmentosa 22 (autosomal recessive);

COM

In two families, homozygosity mapping, haplotype analysis, and linkage data mapped the disease locus (RP22) in an approximately 16-cM region between D16S287 and D16S420 on Chr 16p12. No mutation has been found by direct sequencing in the mu crystallin gene (GEM:16p1311/CRYM), which maps in the critical region (Finckh-1998)."

REF

LIN,LOC "Finckh U &: Genomics, 48, N3, 341-354, 1998

CLA

unknown, basic

LOC

16 p12.3-.1

MIM

MIM: 602594

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