Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F (vol 10, pg 1709, 2001)

Alagramam, KN Yuan, HJ Kuehn, MH Murcia, CL Wayne, S Srisailpathy, CRS Lowry, RB Knaus, R Van Laer, L Bernier, FP Schwartz, S Lee, C Morton, CC Mullins, RF Ramesh, A Van Camp, G Hageman, GS Woychik, RP Smith, RJH

Kn. Alagramam et al., Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F (vol 10, pg 1709, 2001), HUM MOL GEN, 10(22), 2001, pp. 2603-2603

1

Molecular Biology & Genetics

HUMAN MOLECULAR GENETICS

09646906 → ACNP

10

22

2001

2603 - 2603

ISI

0964-6906(20011015)10:22<2603:MITNPP>2.0.ZU;2-X