Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis (Q28145773)
scientific article (publication date: June 2000)
Language:
Current Data About Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis
(P31) (Q13442814)

(P304) 828-31

(P407) (Q1860)

(P433) 6

(P478) 136

(P577) +2000-06-00T00:00:00Z

(P921) (Q498916)
(P887)

(Q24975508)
(P887)

(P1433) (Q7743611)

(P1476) "Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis" (language: en)

(P2093) R Betz
(P1545) 1

C Rensing
(P1545) 2

E Otto
(P1545) 3

A Mincheva
(P1545) 4

D Zehnder
(P1545) 5

P Lichter
(P1545) 6

F Hildebrandt
(P1545) 7

other details
description scientific article (publication date: June 2000)

External Links
(P356) 10.1067/MPD.2000.106225
(P698) 10839884