Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB

A. A. Bergen; P. Kestelyn; M. Leys; F. Meire

doi:https://doi.org/10.1136/jmg.31.7.580

Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB

A. A. Bergen, P. Kestelyn, M. Leys, F. Meire

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Research output: Contribution to journal › Comment/Letter to the editor › Academic

12 Citations (Scopus)

Abstract

The gene for complete congenital stationary night blindness (CSNB1) has been assigned to the Xp11.3 region. However, little evidence has been provided for the assignment of the incomplete congenital stationary night blindness gene (CSNB2). Here we present the clinical and molecular data from a CSNB2 family which show a key recombinant assigning the CSNB2 gene proximal to MAOB

Original language	English
Pages (from-to)	580-582
Journal	Journal of medical genetics
Volume	31
Issue number	7
DOIs	https://doi.org/10.1136/jmg.31.7.580
Publication status	Published - 1994

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https://doi.org/10.1136/jmg.31.7.580

Cite this

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title = "Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB",

abstract = "The gene for complete congenital stationary night blindness (CSNB1) has been assigned to the Xp11.3 region. However, little evidence has been provided for the assignment of the incomplete congenital stationary night blindness gene (CSNB2). Here we present the clinical and molecular data from a CSNB2 family which show a key recombinant assigning the CSNB2 gene proximal to MAOB",

author = "Bergen, {A. A.} and P. Kestelyn and M. Leys and F. Meire",

year = "1994",

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T1 - Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB

AU - Bergen, A. A.

AU - Kestelyn, P.

AU - Leys, M.

AU - Meire, F.

PY - 1994

Y1 - 1994

N2 - The gene for complete congenital stationary night blindness (CSNB1) has been assigned to the Xp11.3 region. However, little evidence has been provided for the assignment of the incomplete congenital stationary night blindness gene (CSNB2). Here we present the clinical and molecular data from a CSNB2 family which show a key recombinant assigning the CSNB2 gene proximal to MAOB

AB - The gene for complete congenital stationary night blindness (CSNB1) has been assigned to the Xp11.3 region. However, little evidence has been provided for the assignment of the incomplete congenital stationary night blindness gene (CSNB2). Here we present the clinical and molecular data from a CSNB2 family which show a key recombinant assigning the CSNB2 gene proximal to MAOB

U2 - https://doi.org/10.1136/jmg.31.7.580

DO - https://doi.org/10.1136/jmg.31.7.580

M3 - Comment/Letter to the editor

C2 - 7966198

SN - 0022-2593

VL - 31

SP - 580

EP - 582

JO - Journal of medical genetics

JF - Journal of medical genetics

IS - 7

ER -